A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4838n100



Internal ID22790925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112379370..112395969hg38UCSC Ensembl
chr3:112098217..112114816hg19UCSC Ensembl
chr3:113580907..113597506hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg3816600
hg1916600
hg1816600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006537, nsv1004948, nsv1007459, nsv999904, nsv1010410, nsv1011313
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4838n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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