A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8381n54



Internal ID22776276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75370585..75500011hg38UCSC Ensembl
chr3:75419736..75549162hg19UCSC Ensembl
chr3:75502426..75631852hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38129427
hg19129427
hg18129427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv590663, nsv590646, nsv590657, nsv590647, nsv590656
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8381n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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