A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520067



Internal ID15100674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98164879..98216260hg38UCSC Ensembl
Innerchr9:100927161..100978542hg19UCSC Ensembl
Innerchr9:99966982..100018363hg18UCSC Ensembl
Innerchr9:98006716..98058097hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3851382
hg1951382
hg1851382
hg1751382
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697204
Samples
Known GenesCORO2A, TBC1D2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520067
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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