A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208298



Internal ID20775338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201965349..202002602hg38UCSC Ensembl
chr2:202830072..202867325hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3837254
hg1937254
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354458
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208298
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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