A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705327



Internal ID15441979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23073970..23087927hg38UCSC Ensembl
Innerchr9:23073969..23087926hg19UCSC Ensembl
Innerchr9:23063969..23077926hg18UCSC Ensembl
Innerchr9:23063969..23077926hg17UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3813958
hg1913958
hg1813958
hg1713958
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)nssv705327
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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