A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202525



Internal ID20769565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:239401681..239406102hg38UCSC Ensembl
chr1:239564981..239569402hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg384422
hg194422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324667
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202525
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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