A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18279020



Internal ID20846060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91298298..91299829hg38UCSC Ensembl
chr8:92310526..92312057hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381532
hg191532
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573061
Supporting Variants
Samples
Known GenesSLC26A7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18279020
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