A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498883



Internal ID275866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63964253..63964680hg38UCSC Ensembl
chr11:63731725..63732152hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046679
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498883
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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