A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552878



Internal ID15993601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:831779..836444hg38UCSC Ensembl
Innerchr11:831779..836444hg19UCSC Ensembl
Innerchr11:821779..826444hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384666
hg194666
hg184666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763573
Samples
Known GenesCD151, EFCAB4A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552878
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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