A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580098



Internal ID16020821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53429042..53519471hg38UCSC Ensembl
Innerchr19:53932295..54022725hg19UCSC Ensembl
Innerchr19:58624107..58714537hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3890430
hg1990431
hg1890431
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6537n54
Supporting Variantsnssv1150174
Samples1780854480_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)nsv580098
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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