A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579676



Internal ID16367085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42813916..43089269hg38UCSC Ensembl
Innerchr19:43318068..43593421hg19UCSC Ensembl
Innerchr19:48009908..48285261hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38275354
hg19275354
hg18275354
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6470n54
Supporting Variantsnssv899680
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579676
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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