A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653621



Internal ID15390273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:132021336..132024643hg38UCSC Ensembl
Innerchr3:131740180..131743487hg19UCSC Ensembl
Innerchr3:133222870..133226177hg18UCSC Ensembl
Innerchr3:133222878..133226185hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg383308
hg193308
hg183308
hg173308
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)nssv653621
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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