A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500026



Internal ID276975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:122826364..122846364hg38UCSC Ensembl
chr11:122697072..122717072hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3820001
hg1920001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053332
Samples
Known GenesCRTAM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500026
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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