A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559911



Internal ID332930
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 StatusM
Merged Variants
Supporting Variantsnssv17711296
Samples
Known GenesPIK3R6
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559911
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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