A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657833



Internal ID15047799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55641224hg38UCSC Ensembl
Innerchr11:55371021..55408700hg19UCSC Ensembl
Innerchr11:55127597..55165276hg18UCSC Ensembl
Innerchr11:55127597..55165276hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3837680
hg1937680
hg1837680
hg1737680
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517440
Supporting Variants
Samples
Known GenesOR4C11, OR4P4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657833
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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