A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509397



Internal ID286051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68328550..68328600hg38UCSC Ensembl
chr11:68096018..68096068hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046327
Samples
Known GenesLRP5
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509397
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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