A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553357



Internal ID16340766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:6094808..6100202hg38UCSC Ensembl
Innerchr11:6116038..6121432hg19UCSC Ensembl
Innerchr11:6072614..6078008hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg385395
hg195395
hg185395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1624n54
Supporting Variantsnssv766311, nssv766310
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553357
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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