A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580267



Internal ID16020990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54751585..54766285hg38UCSC Ensembl
Innerchr19:55263037..55277737hg19UCSC Ensembl
Innerchr19:59954849..59969549hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3814701
hg1914701
hg1814701
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6567n54
Supporting Variantsnssv901677
Samples
Known GenesKIR2DL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580267
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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