A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703431



Internal ID15093397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:21475090..21533927hg38UCSC Ensembl
Innerchr10:21764019..21822856hg19UCSC Ensembl
Innerchr10:21804025..21862862hg18UCSC Ensembl
Innerchr10:21804025..21862862hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3858838
hg1958838
hg1858838
hg1758838
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527055
Supporting Variants
Samples
Known GenesCASC10, MIR1915, SKIDA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703431
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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