A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233187



Internal ID20800227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91848845..91850371hg38UCSC Ensembl
chr10:93608602..93610128hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg381527
hg191527
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6576964
Supporting Variants
Samples
Known GenesTNKS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233187
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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