A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229391



Internal ID20796431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115876617..115890557hg38UCSC Ensembl
chr10:117636128..117650068hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3813941
hg1913941
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6581110
Supporting Variants
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229391
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0001


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