A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560757



Internal ID333756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35804004..35822928hg38UCSC Ensembl
chr9:35804001..35822925hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3818925
hg1918925
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023673
Samples
Known GenesFAM221B, HINT2, NPR2, SPAG8
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560757
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