A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553467



Internal ID15994190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9497004..9627174hg38UCSC Ensembl
Innerchr11:9518551..9648721hg19UCSC Ensembl
Innerchr11:9475127..9605297hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38130171
hg19130171
hg18130171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv767781
Samples
Known GenesWEE1, ZNF143
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553467
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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