A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16900087



Internal ID841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21792454..21796214hg38UCSC Ensembl
chr1:22118947..22122707hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg383761
hg193761
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5426278
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16900087
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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