A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026080



Internal ID21935423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65126845..65132957hg38UCSC Ensembl
chr17:63122963..63129075hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg386113
hg196113
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631430
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026080
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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