A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355669



Internal ID21013222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5065085..5076604hg38UCSC Ensembl
chr3:5106770..5118289hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3811520
hg1911520
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209377
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355669
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