A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433921



Internal ID21091474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:83089501..83883500hg38UCSC Ensembl
chr8:84001736..84795735hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38794000
hg19794000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229829
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433921
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