A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696817



Internal ID15086783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30478169..30546361hg38UCSC Ensembl
Innerchr9:30478167..30546359hg19UCSC Ensembl
Innerchr9:30468167..30536359hg18UCSC Ensembl
Innerchr9:30468167..30536359hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3868193
hg1968193
hg1868193
hg1768193
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517063
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696817
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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