A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552877



Internal ID15993600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:830817..834781hg38UCSC Ensembl
Innerchr11:830817..834781hg19UCSC Ensembl
Innerchr11:820817..824781hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg383965
hg193965
hg183965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763572
Samples
Known GenesCD151, EFCAB4A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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