A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1634n100



Internal ID22787721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41408612..41936985hg38UCSC Ensembl
chr13:41982748..42511121hg19UCSC Ensembl
chr13:40880748..41409121hg18UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38528374
hg19528374
hg18528374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052436, nsv1051548
Samples
Known GenesMIR5006, OR7E37P, RGCC, VWA8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1634n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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