A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17615763



Internal ID21807810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58143294..58143294hg38UCSC Ensembl
chr15:58435493..58435493hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6094541
Supporting Variants
Samples
Known GenesAQP9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17615763
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer