A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv776859



Internal ID15724129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56317135..56467585hg38UCSC Ensembl
Innerchr11:56084611..56235061hg19UCSC Ensembl
Innerchr11:55841187..55991637hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38150451
hg19150451
hg18150451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555097
Supporting Variants
Samples
Known GenesOR5M9, OR5R1, OR8J1, OR8K1, OR8K3, OR8U1, OR8U8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv776859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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