esv3817864

Organism: Homo sapiens

Study:estd214 (1000 Genomes Consortium Phase 3)
Variant Type:mobile element insertion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:57
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):1000 Genomes Project Consortium et al. 2015

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: 447 SVs from 30 studies. See in: genome view

Remapped(Score: Perfect):37,383,317-37,383,317

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
esv3817864	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
esv3817864	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	37,242,570	37,242,570

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
essv16931184	mobile element insertion	SAMN01091093	Sequencing	Read depth and paired-end mapping	Heterozygous	2,301
essv16931185	mobile element insertion	SAMN00014335	Sequencing	Read depth and paired-end mapping	Heterozygous	2,734
essv16931186	mobile element insertion	SAMN01091133	Sequencing	Read depth and paired-end mapping	Heterozygous	2,963
essv16931187	mobile element insertion	SAMN00255122	Sequencing	Read depth and paired-end mapping	Heterozygous	2,934
essv16931188	mobile element insertion	SAMN00262969	Sequencing	Read depth and paired-end mapping	Heterozygous	3,134
essv16931189	mobile element insertion	SAMN00630209	Sequencing	Read depth and paired-end mapping	Heterozygous	3,050
essv16931190	mobile element insertion	SAMN00630210	Sequencing	Read depth and paired-end mapping	Heterozygous	3,134
essv16931191	mobile element insertion	SAMN00262987	Sequencing	Read depth and paired-end mapping	Heterozygous	3,325
essv16931192	mobile element insertion	SAMN00630244	Sequencing	Read depth and paired-end mapping	Heterozygous	2,890
essv16931193	mobile element insertion	SAMN00630251	Sequencing	Read depth and paired-end mapping	Heterozygous	2,787
essv16931194	mobile element insertion	SAMN01091052	Sequencing	Read depth and paired-end mapping	Heterozygous	3,080
essv16931195	mobile element insertion	SAMN00779937	Sequencing	Read depth and paired-end mapping	Heterozygous	3,210
essv16931196	mobile element insertion	SAMN00779949	Sequencing	Read depth and paired-end mapping	Heterozygous	3,105
essv16931197	mobile element insertion	SAMN01761214	Sequencing	Read depth and paired-end mapping	Homozygous	2,448
essv16931198	mobile element insertion	SAMN01036731	Sequencing	Read depth and paired-end mapping	Heterozygous	3,153
essv16931199	mobile element insertion	SAMN01761282	Sequencing	Read depth and paired-end mapping	Heterozygous	3,186
essv16931200	mobile element insertion	SAMN01761229	Sequencing	Read depth and paired-end mapping	Heterozygous	3,411
essv16931201	mobile element insertion	SAMN01036779	Sequencing	Read depth and paired-end mapping	Heterozygous	3,152
essv16931202	mobile element insertion	SAMN01090784	Sequencing	Read depth and paired-end mapping	Heterozygous	2,819
essv16931203	mobile element insertion	SAMN01036783	Sequencing	Read depth and paired-end mapping	Heterozygous	3,166
essv16931204	mobile element insertion	SAMN01761287	Sequencing	Read depth and paired-end mapping	Heterozygous	3,314
essv16931205	mobile element insertion	SAMN01036821	Sequencing	Read depth and paired-end mapping	Heterozygous	3,308
essv16931206	mobile element insertion	SAMN01761295	Sequencing	Read depth and paired-end mapping	Heterozygous	3,217
essv16931207	mobile element insertion	SAMN01090751	Sequencing	Read depth and paired-end mapping	Heterozygous	3,121
essv16931208	mobile element insertion	SAMN01090847	Sequencing	Read depth and paired-end mapping	Heterozygous	3,095
essv16931209	mobile element insertion	SAMN01090846	Sequencing	Read depth and paired-end mapping	Heterozygous	3,080
essv16931210	mobile element insertion	SAMN01761329	Sequencing	Read depth and paired-end mapping	Heterozygous	2,537
essv16931211	mobile element insertion	SAMN01761334	Sequencing	Read depth and paired-end mapping	Heterozygous	2,513
essv16931212	mobile element insertion	SAMN01090803	Sequencing	Read depth and paired-end mapping	Heterozygous	3,000
essv16931213	mobile element insertion	SAMN01090790	Sequencing	Read depth and paired-end mapping	Heterozygous	3,116
essv16931214	mobile element insertion	SAMN01090820	Sequencing	Read depth and paired-end mapping	Heterozygous	3,024
essv16931215	mobile element insertion	SAMN01090812	Sequencing	Read depth and paired-end mapping	Heterozygous	2,924
essv16931216	mobile element insertion	SAMN01090837	Sequencing	Read depth and paired-end mapping	Heterozygous	3,072
essv16931217	mobile element insertion	SAMN01761266	Sequencing	Read depth and paired-end mapping	Heterozygous	2,677
essv16931218	mobile element insertion	SAMN01090829	Sequencing	Read depth and paired-end mapping	Heterozygous	2,716
essv16931219	mobile element insertion	SAMN00001576	Sequencing	Read depth and paired-end mapping	Heterozygous	2,776
essv16931220	mobile element insertion	SAMN00001584	Sequencing	Read depth and paired-end mapping	Heterozygous	3,369
essv16931221	mobile element insertion	SAMN00001589	Sequencing	Read depth and paired-end mapping	Heterozygous	3,170
essv16931222	mobile element insertion	SAMN00001019	Sequencing	Read depth and paired-end mapping	Heterozygous	3,288
essv16931223	mobile element insertion	SAMN00001627	Sequencing	Read depth and paired-end mapping	Heterozygous	3,105
essv16931224	mobile element insertion	SAMN00001697	Sequencing	Read depth and paired-end mapping	Heterozygous	3,373
essv16931225	mobile element insertion	SAMN00001107	Sequencing	Read depth and paired-end mapping	Heterozygous	2,555
essv16931226	mobile element insertion	SAMN00001110	Sequencing	Read depth and paired-end mapping	Heterozygous	3,124
essv16931227	mobile element insertion	SAMN00001134	Sequencing	Read depth and paired-end mapping	Heterozygous	2,950
essv16931228	mobile element insertion	SAMN00001141	Sequencing	Read depth and paired-end mapping	Heterozygous	3,061
essv16931229	mobile element insertion	SAMN00001156	Sequencing	Read depth and paired-end mapping	Heterozygous	2,984
essv16931230	mobile element insertion	SAMN00001158	Sequencing	Read depth and paired-end mapping	Heterozygous	3,001
essv16931231	mobile element insertion	SAMN00001163	Sequencing	Read depth and paired-end mapping	Heterozygous	2,750
essv16931232	mobile element insertion	SAMN00001181	Sequencing	Read depth and paired-end mapping	Heterozygous	2,491
essv16931233	mobile element insertion	SAMN00001182	Sequencing	Read depth and paired-end mapping	Heterozygous	2,784
essv16931234	mobile element insertion	SAMN00001185	Sequencing	Read depth and paired-end mapping	Heterozygous	3,140
essv16931235	mobile element insertion	SAMN00001187	Sequencing	Read depth and paired-end mapping	Homozygous	2,941
essv16931236	mobile element insertion	SAMN00007743	Sequencing	Read depth and paired-end mapping	Heterozygous	3,114
essv16931237	mobile element insertion	SAMN00007814	Sequencing	Read depth and paired-end mapping	Heterozygous	3,114
essv16931238	mobile element insertion	SAMN00006626	Sequencing	Read depth and paired-end mapping	Heterozygous	3,149
essv16931239	mobile element insertion	SAMN00007876	Sequencing	Read depth and paired-end mapping	Heterozygous	3,092
essv16931240	mobile element insertion	SAMN00006629	Sequencing	Read depth and paired-end mapping	Heterozygous	3,232

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
essv16931184	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931185	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931186	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931187	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931188	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931189	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931190	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931191	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931192	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931193	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931194	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931195	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931196	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931197	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931198	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931199	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931200	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931201	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931202	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931203	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931204	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931205	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931206	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931207	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931208	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931209	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931210	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931211	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931212	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931213	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931214	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931215	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931216	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931217	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931218	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931219	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931220	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931221	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931222	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931223	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931224	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931225	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931226	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931227	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931228	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931229	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931230	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931231	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931232	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931233	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931234	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931235	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931236	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931237	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931238	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931239	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931240	Remapped	Perfect	NC_000023.11:g.373 83317_37383318ins?	GRCh38.p12	First Pass	NC_000023.11	ChrX	37,383,317	37,383,317
essv16931184	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931185	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931186	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931187	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931188	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931189	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931190	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931191	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931192	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931193	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931194	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931195	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931196	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931197	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931198	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931199	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931200	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931201	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931202	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931203	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931204	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931205	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931206	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931207	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931208	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931209	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931210	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931211	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931212	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931213	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931214	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931215	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931216	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931217	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931218	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931219	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931220	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931221	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931222	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931223	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931224	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931225	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570
essv16931226	Submitted genomic		NC_000023.10:g.372 42570_37242571ins?	GRCh37 (hg19)		NC_000023.10	ChrX	37,242,570	37,242,570

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dbVar

Database of genomic structural variation

esv3817864

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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.