A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697076



Internal ID15433728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:107662294..107668058hg38UCSC Ensembl
Innerchr9:110424575..110430339hg19UCSC Ensembl
Innerchr9:109464396..109470160hg18UCSC Ensembl
Innerchr9:107504130..107509894hg17UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg385765
hg195765
hg185765
hg175765
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519833
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697076
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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