A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556444



Internal ID15997167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113318201..113512672hg38UCSC Ensembl
Innerchr11:113188923..113383394hg19UCSC Ensembl
Innerchr11:112694133..112888604hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38194472
hg19194472
hg18194472
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv784580
Samples
Known GenesANKK1, DRD2, MIR4301, TTC12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556444
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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