A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486736



Internal ID264094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135419258..135472010hg38UCSC Ensembl
chr9:138311104..138363856hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3852753
hg1952753
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031256
Samples
Known GenesPPP1R26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486736
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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