A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560309



Internal ID333319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:34644703..34652152hg38UCSC Ensembl
chr17:32971722..32979171hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg387450
hg197450
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17712766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560309
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