A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5533388



Internal ID309278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10866950..10905498hg38UCSC Ensembl
chr16:10960807..10999355hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3838549
hg1938549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704536
Samples
Known GenesCIITA
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5533388
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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