A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423529



Internal ID21081082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80575124..80584701hg38UCSC Ensembl
chr8:81487359..81496936hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg389578
hg199578
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171272
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer