A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451417



Internal ID21108970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104811653..105834977hg38UCSC Ensembl
chr10:106571411..107594735hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg381023325
hg191023325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv882n223
Supporting Variantsnssv18179515
Samples
Known GenesSORCS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451417
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