A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17045169



Internal ID97865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65023467..65036959hg38UCSC Ensembl
chr11:64790939..64804431hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3813493
hg1913493
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6142989
Supporting Variants
Samples
Known GenesARL2-SNX15, SNX15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17045169
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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