A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432237



Internal ID21089790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:21354118..21356403hg38UCSC Ensembl
chr8:21211629..21213914hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg382286
hg192286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432237
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