A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519833



Internal ID15447126
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697076
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519833
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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