A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365493



Internal ID21023046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:110126801..110198600hg38UCSC Ensembl
chr3:109845648..109917447hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3871800
hg1971800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207235
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365493
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