A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162916



Internal ID20729958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109871201..109875400hg38UCSC Ensembl
chr8:110883430..110887629hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427945
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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