A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1659n100



Internal ID22787746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:56393219..56453864hg38UCSC Ensembl
chr13:56967353..57027998hg19UCSC Ensembl
chr13:55865354..55925999hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3860646
hg1960646
hg1860646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048689, nsv1040800
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)dgv1659n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer