A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561161



Internal ID334147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:43130963..43131014hg38UCSC Ensembl
chr11:43152513..43152564hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg386012
hg196012
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043995
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561161
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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