A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580068



Internal ID16020791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:53091553..53120518hg38UCSC Ensembl
Innerchr19:53594806..53623771hg19UCSC Ensembl
Innerchr19:58286618..58315583hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3828966
hg1928966
hg1828966
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901147
Samples
Known GenesZNF160, ZNF415
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580068
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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