A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555152



Internal ID16342561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:60508688..60649888hg38UCSC Ensembl
Innerchr11:60276161..60417361hg19UCSC Ensembl
Innerchr11:60032737..60173937hg18UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38141201
hg19141201
hg18141201
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777117
Samples
Known GenesLINC00301, MS4A13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555152
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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