A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561943



Internal ID334909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:112116581..112116632hg38UCSC Ensembl
chr11:111987304..111987355hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050256
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561943
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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