A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556759



Internal ID329887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66766728..66828043hg38UCSC Ensembl
chr13:67340860..67402175hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3861316
hg1961316
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17692140
Samples
Known GenesPCDH9, PCDH9-AS2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556759
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer