A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5540006



Internal ID314853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44629018..44629101hg38UCSC Ensembl
chr22:45024898..45024981hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17729416
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5540006
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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