A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5536379



Internal ID311871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86830885..86830885hg38UCSC Ensembl
chr1:87296568..87296568hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16905872
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5536379
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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