A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv693754



Internal ID15083720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:32456658..32457560hg38UCSC Ensembl
Innerchr9:32456656..32457558hg19UCSC Ensembl
Innerchr9:32446656..32447558hg18UCSC Ensembl
Innerchr9:32446656..32447558hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38903
hg19903
hg18903
hg17903
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519447
Supporting Variants
Samples
Known GenesDDX58
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv693754
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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