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dbVar

Database of genomic structural variation

nsv473846

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:7

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: 217 SVs from 32 studies. See in: genome view

Remapped(Score: Perfect):148,403,074-148,403,080

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv473846	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	148,403,074	148,403,080
nsv473846	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	148,100,166	148,100,172
nsv473846	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000007.12	Chr7	147,731,099	147,731,105

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3020418	complex substitution	NA12156	Sequencing	Sequence alignment	351

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3020418	Remapped	Perfect	GRCh38.p12	First Pass	NC_000007.14	Chr7	148,403,074	148,403,080
nssv3020418	Remapped	Perfect	GRCh37.p13	First Pass	NC_000007.13	Chr7	148,100,166	148,100,172
nssv3020418	Submitted genomic		NCBI36 (hg18)		NC_000007.12	Chr7	147,731,099	147,731,105

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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