A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675626



Internal ID15065592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55669650hg38UCSC Ensembl
Innerchr11:55371021..55437126hg19UCSC Ensembl
Innerchr11:55127597..55193702hg18UCSC Ensembl
Innerchr11:55127597..55193702hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3866106
hg1966106
hg1866106
hg1766106
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)nssv675626
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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