A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3658n100



Internal ID22789745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54218406..54270335hg38UCSC Ensembl
chr19:54722275..54774189hg19UCSC Ensembl
chr19:59414087..59466001hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3851930
hg1951915
hg1851915
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1061991, nsv1066188, nsv1061698, nsv1063558
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)dgv3658n100
Frequency
Sample Size11257
Observed Gain24
Observed Loss8
Observed Complex0
Frequencyn/a


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