A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167126



Internal ID20734166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23223189..23224552hg38UCSC Ensembl
chr8:23080702..23082065hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426255
Supporting Variants
Samples
Known GenesTNFRSF10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167126
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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