A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586496



Internal ID20959567
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 StatusM
Merged Variants
Supporting Variantsnssv18225387
Samples
Known GenesATRNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586496
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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