A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5537469



Internal ID312730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64386862..64386899hg38UCSC Ensembl
chr11:64154334..64154371hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046721
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5537469
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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