A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560860



Internal ID333855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:140338094..140343665hg38UCSC Ensembl
chr8:141348193..141353764hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg385572
hg195572
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17017610
Samples
Known GenesTRAPPC9
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560860
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