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dbVar

Database of genomic structural variation

nsv498760

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:5,443

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: 168 SVs from 42 studies. See in: genome view

Remapped(Score: Perfect):66,166,427-66,171,869

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv498760	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	66,166,427	66,171,869
nsv498760	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	65,933,898	65,939,340
nsv498760	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000011.8	Chr11	65,690,474	65,695,916

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv586538	copy number loss	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv586538	Remapped	Perfect	NC_000011.10:g.661 66427_66171869del	GRCh38.p12	First Pass	NC_000011.10	Chr11	66,166,427	66,171,869
nssv586538	Remapped	Perfect	NC_000011.9:g.6593 3898_65939340del	GRCh37.p13	First Pass	NC_000011.9	Chr11	65,933,898	65,939,340
nssv586538	Submitted genomic		NC_000011.8:g.6569 0474_65695916del	NCBI36 (hg18)		NC_000011.8	Chr11	65,690,474	65,695,916

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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