A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633497



Internal ID7020306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108058361..108068890hg38UCSC Ensembl
chr13:108710709..108721238hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3810530
hg1910530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14892493
SamplesHG02461
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633497
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