A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579437



Internal ID16020160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36353530..36354506hg38UCSC Ensembl
Innerchr19:36844432..36845408hg19UCSC Ensembl
Innerchr19:41536272..41537248hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38977
hg19977
hg18977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6427n54
Supporting Variantsnssv899098, nssv899099
Samples
Known GenesZFP14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579437
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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