A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5408875



Internal ID188198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59448075..59448126hg38UCSC Ensembl
chr11:59215548..59215599hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38141
hg19141
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045508
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5408875
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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