A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697096



Internal ID15433748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11813745..11985139hg38UCSC Ensembl
Innerchr9:11813745..11985139hg19UCSC Ensembl
Innerchr9:11803745..11975139hg18UCSC Ensembl
Innerchr9:11803745..11975139hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38171395
hg19171395
hg18171395
hg17171395
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517379
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697096
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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