A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539559



Internal ID314489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68334662..68334662hg38UCSC Ensembl
chr11:68102130..68102130hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38351
hg19351
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046329
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539559
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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