A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426326



Internal ID205263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44176598..44176649hg38UCSC Ensembl
chr22:44572478..44572529hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729388
Samples
Known GenesPARVG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426326
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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