A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572459



Internal ID16013182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46381084..46505480hg38UCSC Ensembl
Innerchr16:46386457..46539392hg19UCSC Ensembl
Innerchr16:44943958..45096893hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg38124397
hg19152936
hg18152936
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5101n54
Supporting Variantsnssv856518
Samples
Known GenesANKRD26P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572459
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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