A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17607424



Internal ID21799471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28326290..28465083hg38UCSC Ensembl
chr15:28571436..28710229hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38138794
hg19138794
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6109395
Supporting Variants
Samples
Known GenesGOLGA8F, GOLGA8G, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17607424
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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