A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226559



Internal ID20793599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:40919663..40919911hg38UCSC Ensembl
chr13:41493799..41494047hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38249
hg19249
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6578411
Supporting Variants
Samples
Known GenesSUGT1P3, TPTE2P5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226559
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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