A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3661n100



Internal ID22789748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54249470..54336316hg38UCSC Ensembl
chr19:54753328..54847587hg19UCSC Ensembl
chr19:59445140..59539399hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3886847
hg1994260
hg1894260
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063856, nsv1064692
Samples
Known GenesLILRA3, LILRA4, LILRA5, LILRB2, LILRB5, MIR4752
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3661n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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