A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv681680



Internal ID15418332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11879832..12067914hg38UCSC Ensembl
Innerchr9:11879832..12067914hg19UCSC Ensembl
Innerchr9:11869832..12057914hg18UCSC Ensembl
Innerchr9:11869832..12057914hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38188083
hg19188083
hg18188083
hg17188083
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)nssv681680
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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