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dbVar

Database of genomic structural variation

nsv1159610

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: 216 SVs from 20 studies. See in: genome view

Remapped(Score: Perfect):100,134,362-100,134,362

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nsv1159610	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	100,134,362	100,134,362	-
nsv1159610	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	54,337,212	54,337,212	-
nsv1159610	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	100,786,616	100,786,616	-
nsv1159610	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	54,371,124	54,371,124	-

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv4024607	interchromosomal translocation	KWS1	Sequencing	Read depth and paired-end mapping	22,470

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop	strand
nssv4024607	Remapped	Perfect	GRCh38.p12	First Pass	NC_000013.11	Chr13	100,134,362	100,134,362	-
nssv4024607	Remapped	Perfect	GRCh38.p12	First Pass	NC_000016.10	Chr16	54,337,212	54,337,212	-
nssv4024607	Submitted genomic		GRCh37 (hg19)		NC_000013.10	Chr13	100,786,616	100,786,616	-
nssv4024607	Submitted genomic		GRCh37 (hg19)		NC_000016.9	Chr16	54,371,124	54,371,124	-

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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