A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450967



Internal ID21108520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49382839..49385493hg38UCSC Ensembl
chr10:50590885..50593539hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg382655
hg192655
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185201
Samples
Known GenesDRGX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450967
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