A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501181



Internal ID278089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127135958..127142107hg38UCSC Ensembl
chr11:127005853..127012002hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg386150
hg196150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051545
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501181
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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