A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669540



Internal ID15059506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:21813855..21938800hg38UCSC Ensembl
Innerchr1:22140348..22265293hg19UCSC Ensembl
Innerchr1:22012935..22137880hg18UCSC Ensembl
Innerchr1:21885654..22010599hg17UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38124946
hg19124946
hg18124946
hg17124946
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515659
Supporting Variants
Samples
Known GenesHSPG2, LDLRAD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669540
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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