A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205580



Internal ID20772620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157478426..157495247hg38UCSC Ensembl
chr2:158334938..158351759hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3816822
hg1916822
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351039
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205580
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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