A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6563n54



Internal ID22774458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54519000..54645591hg38UCSC Ensembl
chr19:55030183..55157042hg19UCSC Ensembl
chr19:59721995..59848854hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38126592
hg19126860
hg18126860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580238, nsv580239
SamplesHGDP01242, HGDP00388, HGDP00957
Known GenesKIR3DX1, LILRA1, LILRA2, LILRB1, MIR8061
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6563n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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