A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3657n100



Internal ID22789744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54215071..54282373hg38UCSC Ensembl
chr19:54718940..54786228hg19UCSC Ensembl
chr19:59410752..59478040hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3867303
hg1967289
hg1867289
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056881, nsv1055860
Samples
Known GenesLILRA6, LILRB2, LILRB3, 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)dgv3657n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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