A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509183



Internal ID285847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65009206..65018777hg38UCSC Ensembl
chr11:64776678..64786249hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg389572
hg199572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045165
Samples
Known GenesARL2, ARL2-SNX15, MIR6879
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509183
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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