A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578936



Internal ID16019659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20651291..20866398hg38UCSC Ensembl
Innerchr19:20834097..21049204hg19UCSC Ensembl
Innerchr19:20625937..20841044hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38215108
hg19215108
hg18215108
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6318n54
Supporting Variantsnssv896566
Samples
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578936
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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