A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200415



Internal ID20767455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151333454..151334262hg38UCSC Ensembl
chr1:151305930..151306738hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38809
hg19809
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200415
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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