A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6013825



Internal ID21923168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120733283..120734113hg38UCSC Ensembl
chr10:122492795..122493625hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38831
hg19831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17588021
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6013825
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