A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18237322



Internal ID20804362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34915337..34915821hg38UCSC Ensembl
chr15:35207538..35208022hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6584649
Supporting Variants
Samples
Known GenesAQR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18237322
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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