A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579120



Internal ID16366529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27241092..27249967hg38UCSC Ensembl
Innerchr19:27732000..27740875hg19UCSC Ensembl
Innerchr19:32423840..32432715hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg388876
hg198876
hg188876
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv897029, nssv897030
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579120
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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