A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6547n54



Internal ID22774442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:54218061..54233134hg38UCSC Ensembl
chr19:54721930..54737010hg19UCSC Ensembl
chr19:59413742..59428822hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3815074
hg1915081
hg1815081
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv580157, nsv580152, nsv580151
Samples
Known GenesLILRB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6547n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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