A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6029392



Internal ID21938735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112150874..112151161hg38UCSC Ensembl
chr13:112805188..112805475hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38288
hg19288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17611289
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6029392
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