A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432347



Internal ID211091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:11787234..11787271hg38UCSC Ensembl
chrUn_gl000221:107158..107195hg19UCSC Ensembl
Cytoband
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 Variantsnssv17727405
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432347
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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