A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225387



Internal ID20792427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115484016..115486447hg38UCSC Ensembl
chr10:117243526..117245957hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382432
hg192432
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6586496
Supporting Variants
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225387
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00043


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