A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257026



Internal ID20824066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:192950663..195433226hg38UCSC Ensembl
chr2:193815389..196297950hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg382482564
hg192482562
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549949
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257026
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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