A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578927



Internal ID16019650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20644064..20807067hg38UCSC Ensembl
Innerchr19:20826870..20989873hg19UCSC Ensembl
Innerchr19:20618710..20781713hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38163004
hg19163004
hg18163004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6319n54
Supporting Variantsnssv896545, nssv896542, nssv896544, nssv896543
Samples
Known GenesZNF626
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578927
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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