A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6571n54



Internal ID20139995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54766285..54774991hg38UCSC Ensembl
chr19:55277737..55286443hg19UCSC Ensembl
chr19:59969549..59978255hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg388707
hg198707
hg188707
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580288, nsv580285
Samples
Known GenesKIR2DL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6571n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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