A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580083



Internal ID16367492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53372855..53445133hg38UCSC Ensembl
Innerchr19:53876108..53948386hg19UCSC Ensembl
Innerchr19:58567920..58640198hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3872279
hg1972279
hg1872279
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6535n54
Supporting Variantsnssv901161
Samples
Known GenesTPM3P9, ZNF525, ZNF761, ZNF765
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580083
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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