A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700734



Internal ID15437386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163257312..163868181hg38UCSC Ensembl
Innerchr3:162975100..163585969hg19UCSC Ensembl
Innerchr3:164457794..165068663hg18UCSC Ensembl
Innerchr3:164457802..165068671hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38610870
hg19610870
hg18610870
hg17610870
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524743
Supporting Variants
Samples
Known GenesCT64
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700734
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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