A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv763n223



Internal ID22803731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62919201..62932400hg38UCSC Ensembl
chr10:64678961..64692160hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3813200
hg1913200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6449836, nsv6449357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv763n223
Frequency
Sample Size19652
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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