A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365138



Internal ID21022691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159906895..159907598hg38UCSC Ensembl
chr3:159624684..159625387hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38704
hg19704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094728
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365138
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