A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579119



Internal ID16366528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:27241092..27247939hg38UCSC Ensembl
Innerchr19:27732000..27738847hg19UCSC Ensembl
Innerchr19:32423840..32430687hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg386848
hg196848
hg186848
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6360n54
Supporting Variantsnssv897028
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579119
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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