A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202708



Internal ID20769748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:226331597..226341891hg38UCSC Ensembl
chr1:226519298..226529592hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg3810295
hg1910295
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329974
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202708
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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