A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166462



Internal ID20733502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138597626..138615581hg38UCSC Ensembl
chr8:139609869..139627824hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3817956
hg1917956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430897
Supporting Variants
Samples
Known GenesCOL22A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166462
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