A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521491



Internal ID15102098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:12932824..12934723hg38UCSC Ensembl
Innerchr10:12974824..12976723hg19UCSC Ensembl
Innerchr10:13014830..13016729hg18UCSC Ensembl
Innerchr10:13014830..13016729hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381900
hg191900
hg181900
hg171900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698101
Samples
Known GenesCCDC3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521491
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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