A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3660n100



Internal ID20155276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54226329..54340836hg38UCSC Ensembl
chr19:54730202..54852107hg19UCSC Ensembl
chr19:59422014..59543919hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg38114508
hg19121906
hg18121906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060997, nsv1058409, nsv1056066, nsv1061223, nsv1060719, nsv1059726, nsv1066892, nsv1065024, nsv1066267
Samples
Known GenesLILRA3, LILRA4, LILRA5, LILRA6, 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)dgv3660n100
Frequency
Sample Size29084
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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