A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4911n100



Internal ID22790998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:140605170..140745944hg38UCSC Ensembl
chr3:140324012..140464786hg19UCSC Ensembl
chr3:141806702..141947476hg18UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38140775
hg19140775
hg18140775
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv997694, nsv1008123
Samples
Known GenesTRIM42
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4911n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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