A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555147



Internal ID15995870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59023155..59134290hg38UCSC Ensembl
Innerchr11:58790628..58901763hg19UCSC Ensembl
Innerchr11:58547204..58658339hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38111136
hg19111136
hg18111136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174800
SamplesHGDP00601
Known GenesFAM111B, LOC283194
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555147
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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