A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580338



Internal ID16021061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54863187..54866553hg38UCSC Ensembl
Innerchr19:55374642..55378008hg19UCSC Ensembl
Innerchr19:60066454..60069820hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383367
hg193367
hg183367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901804
Samples
Known GenesKIR3DL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580338
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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