A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698694



Internal ID15435346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:90704349..90706612hg38UCSC Ensembl
Innerchr9:93466631..93468894hg19UCSC Ensembl
Innerchr9:92506451..92508714hg18UCSC Ensembl
Innerchr9:90546185..90548448hg17UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382264
hg192264
hg182264
hg172264
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523018
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698694
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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