A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228781



Internal ID20795821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137324055..137350846hg38UCSC Ensembl
chr8:138336298..138363089hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3826792
hg1926792
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228781
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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