A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555150



Internal ID15995873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60046814..60207927hg38UCSC Ensembl
Innerchr11:59814287..59975400hg19UCSC Ensembl
Innerchr11:59570863..59731976hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38161114
hg19161114
hg18161114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174801
SamplesHGDP00685
Known GenesMS4A2, MS4A3, MS4A6A, OOSP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555150
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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