A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5423976



Internal ID202982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86802230..86809894hg38UCSC Ensembl
chr1:87267913..87275577hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg387665
hg197665
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5423976
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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