A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555665



Internal ID16343074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86519856..86706511hg38UCSC Ensembl
Innerchr11:86230898..86417553hg19UCSC Ensembl
Innerchr11:85908546..86095201hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg38186656
hg19186656
hg18186656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779959
Samples
Known GenesME3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555665
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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