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dbVar

Database of genomic structural variation

nsv475161

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:438

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: 150 SVs from 38 studies. See in: genome view

Remapped(Score: Perfect):65,524,270-65,524,707

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv475161	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000010.11	Chr10	65,524,270	65,524,707
nsv475161	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	67,284,028	67,284,465
nsv475161	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000010.9	Chr10	66,954,034	66,954,471

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3018580	complex substitution	NA19240	Sequencing	Sequence alignment	627

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3018580	Remapped	Perfect	GRCh38.p12	First Pass	NC_000010.11	Chr10	65,524,270	65,524,707
nssv3018580	Remapped	Perfect	GRCh37.p13	First Pass	NC_000010.10	Chr10	67,284,028	67,284,465
nssv3018580	Submitted genomic		NCBI36 (hg18)		NC_000010.9	Chr10	66,954,034	66,954,471

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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