A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672881



Internal ID15062847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30251635..30378773hg38UCSC Ensembl
Innerchr9:30251633..30378771hg19UCSC Ensembl
Innerchr9:30241633..30368771hg18UCSC Ensembl
Innerchr9:30241633..30368771hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38127139
hg19127139
hg18127139
hg17127139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672881
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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