A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375579



Internal ID21033132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23028267..23065576hg38UCSC Ensembl
chr3:23069758..23107067hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3837310
hg1937310
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210421
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375579
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