A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5432921



Internal ID211650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121691910..121691934hg38UCSC Ensembl
chr11:121562618..121562642hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5432921
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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