A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6031345



Internal ID21940688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78920969..78923536hg38UCSC Ensembl
chr15:79213311..79215878hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382568
hg192568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17610665
Samples
Known GenesCTSH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6031345
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