A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578804



Internal ID16366213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20040448..20185384hg38UCSC Ensembl
Innerchr19:20151257..20296193hg19UCSC Ensembl
Innerchr19:20012257..20157193hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38144937
hg19144937
hg18144937
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896161
Samples
Known GenesZNF486, ZNF90
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578804
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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