A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4840n100



Internal ID20156456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:112407084..112559957hg38UCSC Ensembl
chr3:112125931..112278804hg19UCSC Ensembl
chr3:113608621..113761494hg18UCSC Ensembl
Cytoband3q13.2
Allele length
AssemblyAllele length
hg38152874
hg19152874
hg18152874
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998309, nsv1003936
Samples
Known GenesATG3, BTLA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4840n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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