A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8385n54



Internal ID22776280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75431963..75869718hg38UCSC Ensembl
chr3:75481114..75918869hg19UCSC Ensembl
chr3:75563804..76001559hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38437756
hg19437756
hg18437756
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590701, nsv590711
Samples
Known GenesFAM86DP, FLJ20518, FRG2C, LINC00960, MIR1324, MIR4273, ZNF717
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8385n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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