A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553536



Internal ID15994259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11841863..11854702hg38UCSC Ensembl
Innerchr11:11863410..11876249hg19UCSC Ensembl
Innerchr11:11819986..11832825hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3812840
hg1912840
hg1812840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1655n54
Supporting Variantsnssv768177, nssv768176
Samples
Known GenesUSP47
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553536
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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