A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170542



Internal ID20737582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67586078..67586809hg38UCSC Ensembl
chr8:68498313..68499044hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428545
Supporting Variants
Samples
Known GenesCPA6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170542
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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