A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512132



Internal ID288699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:26586806..26589289hg38UCSC Ensembl
chr11:26608353..26610836hg19UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg382484
hg192484
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042659
Samples
Known GenesANO3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512132
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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