A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580085



Internal ID16020808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53396620..53479458hg38UCSC Ensembl
Innerchr19:53899873..53982712hg19UCSC Ensembl
Innerchr19:58591685..58674524hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3882839
hg1982840
hg1882840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6536n54
Supporting Variantsnssv901163
Samples
Known GenesTPM3P9, ZNF761, ZNF765, ZNF813
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580085
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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