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dbVar

Database of genomic structural variation

nsv473744

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:4

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: 137 SVs from 36 studies. See in: genome view

Remapped(Score: Perfect):58,965,942-58,965,945

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv473744	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	58,965,942	58,965,945
nsv473744	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	59,359,723	59,359,726
nsv473744	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000012.10	Chr12	57,645,990	57,645,993

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv3018931	complex substitution	NA19129	Sequencing	Sequence alignment	871

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv3018931	Remapped	Perfect	GRCh38.p12	First Pass	NC_000012.12	Chr12	58,965,942	58,965,945
nssv3018931	Remapped	Perfect	GRCh37.p13	First Pass	NC_000012.11	Chr12	59,359,723	59,359,726
nssv3018931	Submitted genomic		NCBI36 (hg18)		NC_000012.10	Chr12	57,645,990	57,645,993

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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