A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3632593



Internal ID7019403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68369240..68466526hg38UCSC Ensembl
chr13:68943372..69040658hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3897287
hg1997287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14782684
SamplesHG03838
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3632593
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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