A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703509



Internal ID15093475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:26169872..26187345hg38UCSC Ensembl
Innerchr2:26392741..26410214hg19UCSC Ensembl
Innerchr2:26246245..26263718hg18UCSC Ensembl
Innerchr2:26304392..26321865hg17UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3817474
hg1917474
hg1817474
hg1717474
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520638
Supporting Variants
Samples
Known GenesGAREML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703509
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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