A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421998



Internal ID21079551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114543784..114608996hg38UCSC Ensembl
chr8:115556013..115621225hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3865213
hg1965213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421998
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