A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562939



Internal ID335878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29462108..29462159hg38UCSC Ensembl
chr11:29483655..29483706hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg386017
hg196017
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043061
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562939
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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