A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv12091n54



Internal ID20145515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39349476..39498641hg38UCSC Ensembl
chr8:39206995..39356160hg19UCSC Ensembl
chr8:39326152..39475317hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38149166
hg19149166
hg18149166
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv610977, nsv610951, nsv611023, nsv610960
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv12091n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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