A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697192



Internal ID15433844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:88280269..88284712hg38UCSC Ensembl
Innerchr9:90895184..90899627hg19UCSC Ensembl
Innerchr9:90085004..90089447hg18UCSC Ensembl
Innerchr9:88124738..88129181hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg384444
hg194444
hg184444
hg174444
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520042
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697192
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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