A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676252



Internal ID15066218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55679951hg38UCSC Ensembl
Innerchr11:55371021..55447427hg19UCSC Ensembl
Innerchr11:55127597..55204003hg18UCSC Ensembl
Innerchr11:55127597..55204003hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3876407
hg1976407
hg1876407
hg1776407
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)nssv676252
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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