A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6575n54



Internal ID20139999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54772175..54775402hg38UCSC Ensembl
chr19:55283627..55286854hg19UCSC Ensembl
chr19:59975439..59978666hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg383228
hg193228
hg183228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580307, nsv580306, nsv580312
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6575n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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