A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236792



Internal ID20803832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:18318711..18402598hg38UCSC Ensembl
chr8:18176220..18260108hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3883888
hg1983889
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6434506
Supporting Variants
Samples
Known GenesNAT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236792
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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