A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1734n100



Internal ID22787821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103443768..103520940hg38UCSC Ensembl
chr13:104096118..104173290hg19UCSC Ensembl
chr13:102894119..102971291hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3877173
hg1977173
hg1877173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040554, nsv1036855, nsv1046691
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)dgv1734n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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