A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673443



Internal ID15063409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55655110hg38UCSC Ensembl
Innerchr11:55371021..55422586hg19UCSC Ensembl
Innerchr11:55127597..55179162hg18UCSC Ensembl
Innerchr11:55127597..55179162hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3851566
hg1951566
hg1851566
hg1751566
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517440
Supporting Variants
Samples
Known GenesOR4C11, OR4P4, OR4S2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673443
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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