A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573428



Internal ID16014151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84378422..84455324hg38UCSC Ensembl
Innerchr16:84412028..84488930hg19UCSC Ensembl
Innerchr16:82969529..83046431hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3876903
hg1976903
hg1876903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149335
SamplesHGDP00572
Known GenesATP2C2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573428
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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