A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6568n54



Internal ID20139992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54753949..54775604hg38UCSC Ensembl
chr19:55265401..55287056hg19UCSC Ensembl
chr19:59957213..59978868hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3821656
hg1921656
hg1821656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580273, nsv580274, nsv580279, nsv580269, nsv580275, nsv580278, nsv580276, nsv580277, nsv580270
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6568n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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