A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520589



Internal ID15447882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:31382627..31385151hg38UCSC Ensembl
Innerchr1:31855474..31857998hg19UCSC Ensembl
Innerchr1:31628061..31630585hg18UCSC Ensembl
Innerchr1:31524567..31527091hg17UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg382525
hg192525
hg182525
hg172525
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697507
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520589
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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