A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv685395



Internal ID15075361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55692619hg38UCSC Ensembl
Innerchr11:55371021..55460095hg19UCSC Ensembl
Innerchr11:55127597..55216671hg18UCSC Ensembl
Innerchr11:55127597..55216671hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3889075
hg1989075
hg1889075
hg1789075
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517440
Supporting Variants
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv685395
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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