A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4725n100



Internal ID22790812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41842047..41947832hg38UCSC Ensembl
chr3:41883539..41989324hg19UCSC Ensembl
chr3:41858543..41964328hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38105786
hg19105786
hg18105786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008981, nsv1004339
Samples
Known GenesULK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4725n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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