A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6032045



Internal ID21941388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31373540..31373738hg38UCSC Ensembl
chr13:31947677..31947875hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38199
hg19199
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597659
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6032045
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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