A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580260



Internal ID16020983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54750252..54764062hg38UCSC Ensembl
Innerchr19:55261704..55275514hg19UCSC Ensembl
Innerchr19:59953516..59967326hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3813811
hg1913811
hg1813811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6567n54
Supporting Variantsnssv901668, nssv901669, nssv901667
Samples
Known GenesKIR2DL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580260
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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