A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557796



Internal ID330882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60682422..60682467hg38UCSC Ensembl
chr11:60449895..60449940hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047835
Samples
Known GenesLINC00301
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557796
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer