A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18244987



Internal ID20812027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10710435..10710749hg38UCSC Ensembl
chr19:10821111..10821425hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6596945
Supporting Variants
Samples
Known GenesQTRT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18244987
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