A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556445



Internal ID15997168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113396099..113400106hg38UCSC Ensembl
Innerchr11:113266821..113270828hg19UCSC Ensembl
Innerchr11:112772031..112776038hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg384008
hg194008
hg184008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784581
Samples
Known GenesANKK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556445
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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