A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4780n100



Internal ID22790867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75377944..75451601hg38UCSC Ensembl
chr3:75427095..75500752hg19UCSC Ensembl
chr3:75509785..75583442hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg3873658
hg1973658
hg1873658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009873, nsv1012334, nsv1011350
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4780n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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