A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508635



Internal ID285322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132631427..132634438hg38UCSC Ensembl
chr11:132501322..132504333hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg383012
hg193012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17054503
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508635
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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