A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17606216



Internal ID21798263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67391144..67391710hg38UCSC Ensembl
chr15:67683482..67684048hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6037332
Supporting Variants
Samples
Known GenesIQCH
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17606216
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