A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510079



Internal ID286709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:129862841..129863417hg38UCSC Ensembl
chr11:129732736..129733312hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510079
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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