A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398543



Internal ID21056096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99501201..99536800hg38UCSC Ensembl
chr5:98836905..98872504hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3835600
hg1935600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5836n223
Supporting Variantsnssv18215480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398543
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