A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228406



Internal ID20795446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69098548..69099518hg38UCSC Ensembl
chr10:70858304..70859274hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg38971
hg19971
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6579423
Supporting Variants
Samples
Known GenesSRGN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228406
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