A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578809



Internal ID16019532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:20352186..21528400hg38UCSC Ensembl
Innerchr19:20462995..21711202hg19UCSC Ensembl
Innerchr19:20323995..21503042hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg381176215
hg191248208
hg181179048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149851
SamplesHGDP00598
Known GenesLINC00664, MIR1270-1, MIR1270-2, ZNF429, ZNF430, ZNF431, ZNF493, ZNF626, ZNF708, ZNF714, ZNF737, ZNF738, ZNF826P, ZNF85
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578809
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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