A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553404



Internal ID16340813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7114550..7124807hg38UCSC Ensembl
Innerchr11:7135781..7146038hg19UCSC Ensembl
Innerchr11:7092357..7102614hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810258
hg1910258
hg1810258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv766937
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553404
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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