A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5542626



Internal ID317025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122671153..122671153hg38UCSC Ensembl
chr5:122006848..122006848hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16973414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5542626
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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