A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3655n100



Internal ID22789742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54213432..54250521hg38UCSC Ensembl
chr19:54717301..54754385hg19UCSC Ensembl
chr19:59409113..59446197hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3837090
hg1937085
hg1837085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1065918, nsv1066693, nsv1064055, nsv1061563, nsv1065266
Samples
Known GenesLILRA6, LILRB3, LILRB5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3655n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer