A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222900



Internal ID20789940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:134880215..134999249hg38UCSC Ensembl
chr8:135892458..136011492hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38119035
hg19119035
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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