A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699757



Internal ID15436409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5186159..5210335hg38UCSC Ensembl
Innerchr11:5207389..5231565hg19UCSC Ensembl
Innerchr11:5163965..5188141hg18UCSC Ensembl
Innerchr11:5163965..5188141hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824177
hg1924177
hg1824177
hg1724177
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523914
Supporting Variants
Samples
Known GenesOR51V1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699757
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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