A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697348



Internal ID15434000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:79157231..79158912hg38UCSC Ensembl
Innerchr9:81772146..81773827hg19UCSC Ensembl
Innerchr9:80961966..80963647hg18UCSC Ensembl
Innerchr9:79001700..79003381hg17UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg381682
hg191682
hg181682
hg171682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520323
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697348
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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