A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495394



Internal ID272511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132696442..132705393hg38UCSC Ensembl
chr11:132566337..132575288hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg388952
hg198952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17054511
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495394
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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