A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8384n54



Internal ID22776279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75400984..75523048hg38UCSC Ensembl
chr3:75450135..75572199hg19UCSC Ensembl
chr3:75532825..75654889hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38122065
hg19122065
hg18122065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590692, nsv590680, nsv590694, nsv590696, nsv590693, nsv590682, nsv590681, nsv590695, nsv590673, nsv590670, nsv590679, nsv590699, nsv590684, nsv590671, nsv590683, nsv590672
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8384n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss65
Observed Complex0
Frequencyn/a


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