A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423353



Internal ID21080906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:90455484..90506130hg38UCSC Ensembl
chr8:91467712..91518358hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3850647
hg1950647
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423353
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