A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552932



Internal ID16340341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1333474..1376789hg38UCSC Ensembl
Innerchr11:1354704..1398019hg19UCSC Ensembl
Innerchr11:1311280..1354595hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3843316
hg1943316
hg1843316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174589
Samples1780862067_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552932
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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