A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671660



Internal ID15408312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14565266..14583054hg38UCSC Ensembl
Innerchr2:14705390..14723178hg19UCSC Ensembl
Innerchr2:14622841..14640629hg18UCSC Ensembl
Innerchr2:14655988..14673776hg17UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3817789
hg1917789
hg1817789
hg1717789
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516976
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671660
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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