A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579118



Internal ID16366527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27241092..27246791hg38UCSC Ensembl
Innerchr19:27732000..27737699hg19UCSC Ensembl
Innerchr19:32423840..32429539hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg385700
hg195700
hg185700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6360n54
Supporting Variantsnssv897026, nssv897027
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579118
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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