A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664913



Internal ID15054879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55677392..55836936hg38UCSC Ensembl
Innerchr11:55444868..55604412hg19UCSC Ensembl
Innerchr11:55201444..55360988hg18UCSC Ensembl
Innerchr11:55201444..55360988hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38159545
hg19159545
hg18159545
hg17159545
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)nssv664913
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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