A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040185



Internal ID21949528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113262788..113263143hg38UCSC Ensembl
chr13:113917102..113917457hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17606046
Samples
Known GenesCUL4A, MIR8075
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040185
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