A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693721



Internal ID15430373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132013576..132024643hg38UCSC Ensembl
Innerchr3:131732420..131743487hg19UCSC Ensembl
Innerchr3:133215110..133226177hg18UCSC Ensembl
Innerchr3:133215118..133226185hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3811068
hg1911068
hg1811068
hg1711068
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517016
Supporting Variants
Samples
Known GenesCPNE4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693721
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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