A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692503



Internal ID15429155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23073970..23105082hg38UCSC Ensembl
Innerchr9:23073969..23105081hg19UCSC Ensembl
Innerchr9:23063969..23095081hg18UCSC Ensembl
Innerchr9:23063969..23095081hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3831113
hg1931113
hg1831113
hg1731113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521195
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692503
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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