A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578929



Internal ID16019652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20651291..20798152hg38UCSC Ensembl
Innerchr19:20834097..20980958hg19UCSC Ensembl
Innerchr19:20625937..20772798hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38146862
hg19146862
hg18146862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6319n54
Supporting Variantsnssv896548
Samples
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578929
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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