A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555215



Internal ID15995938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65814108..65909045hg38UCSC Ensembl
Innerchr11:65581579..65676516hg19UCSC Ensembl
Innerchr11:65338155..65433092hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3894938
hg1994938
hg1894938
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777182
Samples
Known GenesCCDC85B, CFL1, CTSW, EFEMP2, FIBP, FOSL1, MUS81, SNX32
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555215
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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