A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578910



Internal ID16019633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20499249..20804744hg38UCSC Ensembl
Innerchr19:20682055..20987550hg19UCSC Ensembl
Innerchr19:20473895..20779390hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38305496
hg19305496
hg18305496
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv896514
Samples
Known GenesZNF626, ZNF737
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578910
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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