A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592784



Internal ID16033507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189648806..189651173hg38UCSC Ensembl
Innerchr3:189366595..189368962hg19UCSC Ensembl
Innerchr3:190849289..190851656hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg382368
hg192368
hg182368
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv983008
Samples
Known GenesTP63
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592784
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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