A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509568



Internal ID286217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112392864..112396582hg38UCSC Ensembl
chr11:112263587..112267305hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg383719
hg193719
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050283
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509568
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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