A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553782



Internal ID16341191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:24168592..24245676hg38UCSC Ensembl
Innerchr11:24190138..24267222hg19UCSC Ensembl
Innerchr11:24146714..24223798hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3877085
hg1977085
hg1877085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768978
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553782
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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