A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580096



Internal ID16020819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53429042..53508130hg38UCSC Ensembl
Innerchr19:53932295..54011384hg19UCSC Ensembl
Innerchr19:58624107..58703196hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3879089
hg1979090
hg1879090
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n54
Supporting Variantsnssv1150169, nssv901177
Samples1780854540_A
Known GenesTPM3P9, ZNF761, ZNF813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580096
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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