A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364169



Internal ID21021722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109224927..109234646hg38UCSC Ensembl
chr3:108943774..108953493hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg389720
hg199720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093363
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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