A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555151



Internal ID15995874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60448972..60472250hg38UCSC Ensembl
Innerchr11:60216445..60239723hg19UCSC Ensembl
Innerchr11:59973021..59996299hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3823279
hg1923279
hg1823279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777116
Samples
Known GenesMS4A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555151
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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