A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17605793



Internal ID21797840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31210160..31214062hg38UCSC Ensembl
chr15:31502363..31506265hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg383903
hg193903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6040444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17605793
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