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dbVar

Database of genomic structural variation

nsv474637

Organism: Homo sapiens

Study:nstd35 (Kidd et al. 2010)
Variant Type:complex substitution
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:354

Description:complex allele - no allele length provided
Publication(s):Kidd et al. 2010

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: 174 SVs from 46 studies. See in: genome view

Remapped(Score: Perfect):65,936,763-65,937,116

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv474637	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	65,936,763	65,937,116
nsv474637	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	66,802,481	66,802,834
nsv474637	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000004.10	Chr4	66,485,076	66,485,429

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3011555	complex substitution	NA18956	Sequencing	Sequence alignment	601

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3011555	Remapped	Perfect	GRCh38.p12	First Pass	NC_000004.12	Chr4	65,936,763	65,937,116
nssv3011555	Remapped	Perfect	GRCh37.p13	First Pass	NC_000004.11	Chr4	66,802,481	66,802,834
nssv3011555	Submitted genomic		NCBI36 (hg18)		NC_000004.10	Chr4	66,485,076	66,485,429

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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