A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409848



Internal ID21067401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115714462..115820425hg38UCSC Ensembl
chr5:115050159..115156122hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg38105964
hg19105964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5904n223
Supporting Variantsnssv18212466
Samples
Known GenesCDO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409848
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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