A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17602859



Internal ID21794906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31208124..31208495hg38UCSC Ensembl
chr15:31500327..31500698hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38372
hg19372
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6025300
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17602859
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