A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688149



Internal ID15078115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55677392..55828837hg38UCSC Ensembl
Innerchr11:55444868..55596313hg19UCSC Ensembl
Innerchr11:55201444..55352889hg18UCSC Ensembl
Innerchr11:55201444..55352889hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38151446
hg19151446
hg18151446
hg17151446
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517440
Supporting Variants
Samples
Known GenesOR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688149
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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