A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498536



Internal ID275526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43860479..43861791hg38UCSC Ensembl
chr11:43882029..43883341hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044978
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498536
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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