A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432335



Internal ID21089888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:80125390..80131197hg38UCSC Ensembl
chr8:81037625..81043432hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385808
hg195808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18171245
Samples
Known GenesTPD52
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432335
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