A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8383n54



Internal ID22776278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75370585..75606894hg38UCSC Ensembl
chr3:75419736..75656045hg19UCSC Ensembl
chr3:75502426..75738735hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38236310
hg19236310
hg18236310
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590662, nsv590654, nsv590652, nsv590651, nsv590653
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8383n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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