A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6569n54



Internal ID20139993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54764062..54778505hg38UCSC Ensembl
chr19:55275514..55289957hg19UCSC Ensembl
chr19:59967326..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 Variants
Supporting Variantsnsv580283, nsv580282
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6569n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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