A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5399666



Internal ID179054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65174890..65174941hg38UCSC Ensembl
chr11:64942361..64942412hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045179
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5399666
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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