A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208261



Internal ID20775301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:198661404..198733534hg38UCSC Ensembl
chr2:199526128..199598258hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3872131
hg1972131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6346893
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208261
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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