A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023015



Internal ID21932358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:65055702..65158652hg38UCSC Ensembl
chr13:65629834..65732784hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38102951
hg19102951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605669
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023015
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