A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579779



Internal ID16367188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43055178..43344645hg38UCSC Ensembl
Innerchr19:43559330..43848797hg19UCSC Ensembl
Innerchr19:48251170..48540637hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38289468
hg19289468
hg18289468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv899807
Samples
Known GenesLOC284344, PSG2, PSG4, PSG5, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer