A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv579819



Internal ID16367228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43158934..43349353hg38UCSC Ensembl
Innerchr19:43663086..43853505hg19UCSC Ensembl
Innerchr19:48354926..48545345hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38190420
hg19190420
hg18190420
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6497n54
Supporting Variantsnssv899868
Samples
Known GenesLOC284344, PRG1, PSG4, PSG5, PSG9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv579819
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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