A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8379n54



Internal ID22776274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75345636..75481744hg38UCSC Ensembl
chr3:75394787..75530895hg19UCSC Ensembl
chr3:75477477..75613585hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38136109
hg19136109
hg18136109
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590644, nsv590643
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8379n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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