A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705522



Internal ID15442174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21364353..21382131hg38UCSC Ensembl
Innerchr2:21587225..21605003hg19UCSC Ensembl
Innerchr2:21440730..21458508hg18UCSC Ensembl
Innerchr2:21498877..21516655hg17UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3817779
hg1917779
hg1817779
hg1717779
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528844
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705522
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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