A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498662



Internal ID275649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59903436..59903511hg38UCSC Ensembl
chr11:59670909..59670984hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498662
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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