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dbVar

Database of genomic structural variation

nsv1159637

Organism: Homo sapiens

Study:nstd106 (Alsmadi et al. 2014)
Variant Type:translocation
Method Type:Sequencing
Submitted on:GRCh37 (hg19)

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

Publication(s):Alsmadi et al. 2014

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: 80 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):50,157,851-50,157,851

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nsv1159637	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	50,157,851	50,157,851	-
nsv1159637	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000022.11	Chr22	42,545,385	42,545,385	-
nsv1159637	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	50,551,634	50,551,634	-
nsv1159637	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000022.10	Chr22	42,941,391	42,941,391	-

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv4024640	interchromosomal translocation	KWS2	Sequencing	Read depth and paired-end mapping	21,718

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nssv4024640	Remapped	Perfect	GRCh38.p12	First Pass	NC_000012.12	Chr12	50,157,851	50,157,851	-
nssv4024640	Remapped	Perfect	GRCh38.p12	First Pass	NC_000022.11	Chr22	42,545,385	42,545,385	-
nssv4024640	Submitted genomic		GRCh37 (hg19)		NC_000012.11	Chr12	50,551,634	50,551,634	-
nssv4024640	Submitted genomic		GRCh37 (hg19)		NC_000022.10	Chr22	42,941,391	42,941,391	-

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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