A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5652802



Internal ID21601107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6784953..6784953hg38UCSC Ensembl
chr17:6688272..6688272hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082117
SamplesHG03125
Known GenesFBXO39
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5652802
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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