A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513922



Internal ID290429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88643959..88644651hg38UCSC Ensembl
chr16:88710367..88711059hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17710562
Samples
Known GenesCYBA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513922
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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