A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4702n100



Internal ID20156318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23366936..23427572hg38UCSC Ensembl
chr3:23408427..23469063hg19UCSC Ensembl
chr3:23383431..23444067hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3860637
hg1960637
hg1860637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010032, nsv1012236
Samples
Known GenesMIR548AC, UBE2E2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4702n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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