A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262434



Internal ID20829474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:122852126..122853757hg38UCSC Ensembl
chr3:122570973..122572604hg19UCSC Ensembl
Cytoband3q21.1
Allele length
AssemblyAllele length
hg381632
hg191632
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568609
Supporting Variants
Samples
Known GenesDIRC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262434
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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