A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501485



Internal ID278384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106108178..106109882hg38UCSC Ensembl
chr11:105978905..105980609hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050572
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501485
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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