A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5547626



Internal ID321454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:10940152..10942197hg38UCSC Ensembl
chrUn_gl000241:15580..17625hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg382046
hg192046
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17727359
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5547626
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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