A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17616037



Internal ID21808084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40244472..40244547hg38UCSC Ensembl
chr15:40536673..40536748hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6036051
Supporting Variants
Samples
Known GenesPAK6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17616037
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