A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235192



Internal ID20802232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23208469..23213451hg38UCSC Ensembl
chr8:23065982..23070964hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg384983
hg194983
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422715
Supporting Variants
Samples
Known GenesTNFRSF10A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235192
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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