A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579722



Internal ID16367131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42870449..43150057hg38UCSC Ensembl
Innerchr19:43374601..43654209hg19UCSC Ensembl
Innerchr19:48066441..48346049hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38279609
hg19279609
hg18279609
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6474n54
Supporting Variantsnssv899745
Samples
Known GenesPSG1, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579722
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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