A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520331



Internal ID15100938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:157140511..157197861hg38UCSC Ensembl
Innerchr3:156858300..156915650hg19UCSC Ensembl
Innerchr3:158340994..158398344hg18UCSC Ensembl
Innerchr3:158341002..158398352hg17UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3857351
hg1957351
hg1857351
hg1757351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702488, nssv673876, nssv662968
Samples
Known GenesCCNL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520331
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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