A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578934



Internal ID16019657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20651291..20818370hg38UCSC Ensembl
Innerchr19:20834097..21001176hg19UCSC Ensembl
Innerchr19:20625937..20793016hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38167080
hg19167080
hg18167080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6319n54
Supporting Variantsnssv896564, nssv896563
Samples
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578934
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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