esv3841222

Organism: Homo sapiens

Study:estd219 (1000 Genomes Consortium Phase 3 Integrated SV)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:49
Validation:Not tested
Clinical Assertions: No
Region Size:77,749

Publication(s):1000 Genomes Consortium Phase 3 Integrated SV

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 932 SVs from 81 studies. See in: genome view

Remapped(Score: Perfect):97,714,801-97,792,549

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3841222	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
esv3841222	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	97,050,505	97,128,253

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv19646147	deletion	HG00106	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,290
essv19646148	deletion	HG00121	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,326
essv19646149	deletion	HG00178	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,406
essv19646150	deletion	HG00179	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,095
essv19646151	deletion	HG00180	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,031
essv19646152	deletion	HG00186	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,391
essv19646153	deletion	HG00252	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,570
essv19646154	deletion	HG00275	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,155
essv19646155	deletion	HG00321	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,384
essv19646156	deletion	HG00323	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,081
essv19646157	deletion	HG00325	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,403
essv19646158	deletion	HG00343	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,020
essv19646159	deletion	HG00344	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,886
essv19646160	deletion	HG00366	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,572
essv19646161	deletion	HG00638	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,281
essv19646162	deletion	HG01060	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,683
essv19646163	deletion	HG01064	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,863
essv19646164	deletion	HG01077	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,787
essv19646165	deletion	HG01111	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,414
essv19646166	deletion	HG01167	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,580
essv19646167	deletion	HG01190	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,469
essv19646168	deletion	HG01191	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,249
essv19646169	deletion	HG01405	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,814
essv19646170	deletion	HG01464	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,831
essv19646171	deletion	HG01495	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,329
essv19646172	deletion	HG01527	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,631
essv19646173	deletion	HG01618	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,073
essv19646174	deletion	HG01632	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,359
essv19646175	deletion	HG01767	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,623
essv19646176	deletion	HG02491	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,369
essv19646177	deletion	HG02655	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,369
essv19646178	deletion	HG02774	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,674
essv19646179	deletion	HG03672	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,546
essv19646180	deletion	HG03756	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,417
essv19646181	deletion	HG03803	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,515
essv19646182	deletion	HG04018	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,180
essv19646183	deletion	NA07357	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,777
essv19646184	deletion	NA11830	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	2,943
essv19646185	deletion	NA12283	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Homozygous	3,365
essv19646186	deletion	NA12340	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,534
essv19646187	deletion	NA12812	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,515
essv19646188	deletion	NA12890	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,371
essv19646189	deletion	NA19648	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,140
essv19646190	deletion	NA20504	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,407
essv19646191	deletion	NA20516	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,702
essv19646192	deletion	NA20753	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,496
essv19646193	deletion	NA20769	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,107
essv19646194	deletion	NA20773	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,348
essv19646195	deletion	NA21107	Sequencing	Paired-end mapping, Read depth, Read depth and paired-end mapping, Split read mapping	Heterozygous	3,587

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv19646147	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646148	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646149	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646150	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646151	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646152	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646153	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646154	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646155	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646156	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646157	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646158	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646159	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646160	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646161	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646162	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646163	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646164	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646165	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646166	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646167	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646168	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646169	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646170	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646171	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646172	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646173	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646174	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646175	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646176	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646177	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646178	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646179	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646180	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646181	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646182	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646183	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646184	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646185	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646186	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646187	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646188	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646189	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646190	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646191	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646192	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646193	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646194	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646195	Remapped	Perfect	NC_000005.10:g.977 14801_97792549del	GRCh38.p12	First Pass	NC_000005.10	Chr5	97,714,801	97,792,549
essv19646147	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646148	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646149	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646150	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646151	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646152	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646153	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646154	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646155	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646156	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646157	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646158	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646159	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646160	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646161	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646162	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646163	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646164	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646165	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646166	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646167	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646168	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646169	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646170	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646171	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646172	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646173	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646174	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646175	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646176	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646177	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646178	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646179	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646180	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646181	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646182	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646183	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646184	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646185	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646186	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646187	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646188	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646189	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646190	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646191	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646192	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646193	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646194	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253
essv19646195	Submitted genomic		NC_000005.9:g.9705 0505_97128253del	GRCh37 (hg19)		NC_000005.9	Chr5	97,050,505	97,128,253

dbVar

Database of genomic structural variation

esv3841222

Links to Other Resources

Genome View

Variant Region Placement Information

Variant Call Information

Variant Call Placement Information

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.