A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495896



Internal ID272991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:113842682..113861000hg38UCSC Ensembl
chr11:113713404..113731722hg19UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3818319
hg1918319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052486
Samples
Known GenesUSP28
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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