A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174790



Internal ID15877136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55679951..55828837hg38UCSC Ensembl
Innerchr11:55447427..55596313hg19UCSC Ensembl
Innerchr11:55204003..55352889hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38148887
hg19148887
hg18148887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555061
Supporting Variants
SamplesHGDP00940
Known GenesOR5D13, OR5D14, OR5D18, OR5L1, OR5L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174790
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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