A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364307



Internal ID21021860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:147768325..147773058hg38UCSC Ensembl
chr3:147486112..147490845hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg384734
hg194734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095765
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364307
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