A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356389



Internal ID21013942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4023139..4052579hg38UCSC Ensembl
chr3:4064823..4094263hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3829441
hg1929441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100932
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356389
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