A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505759



Internal ID282525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65011136..65018701hg38UCSC Ensembl
chr11:64778608..64786173hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387566
hg197566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045167
Samples
Known GenesARL2, ARL2-SNX15, MIR6879
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505759
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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