A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171290



Internal ID20738330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81048723..81054709hg38UCSC Ensembl
chr8:81960958..81966944hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg385987
hg195987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423121
Supporting Variants
Samples
Known GenesPAG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171290
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