A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165001



Internal ID20732041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:127590356..127590736hg38UCSC Ensembl
chr8:128602601..128602981hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg38381
hg19381
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165001
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00061


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