A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580283



Internal ID16021006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54764062..54778505hg38UCSC Ensembl
Innerchr19:55275514..55289957hg19UCSC Ensembl
Innerchr19:59967326..59981769hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3814444
hg1914444
hg1814444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6569n54
Supporting Variantsnssv901699
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580283
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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