A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553566



Internal ID15994289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:16307463..16777497hg38UCSC Ensembl
Innerchr11:16329009..16799044hg19UCSC Ensembl
Innerchr11:16285585..16755620hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38470035
hg19470036
hg18470036
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv768280
Samples
Known GenesC11orf58, SOX6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553566
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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