A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579817



Internal ID16367226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43158934..43341441hg38UCSC Ensembl
Innerchr19:43663086..43845593hg19UCSC Ensembl
Innerchr19:48354926..48537433hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38182508
hg19182508
hg18182508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6497n54
Supporting Variantsnssv899866, nssv899864, nssv899865
Samples
Known GenesLOC284344, PSG4, PSG5, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579817
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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