A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17711296



Internal ID134962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8830930..8840950hg38UCSC Ensembl
chr17:8734247..8744267hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3810021
hg1910021
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5559911
Supporting Variants
Samples
Known GenesPIK3R6
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17711296
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.007961


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