A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561493



Internal ID334472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:32053959..32209546hg38UCSC Ensembl
chr17:30380978..30536565hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38155588
hg19155588
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712622
Samples
Known GenesARGFXP2, RHOT1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561493
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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