A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248833



Internal ID20815873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179850073..179850275hg38UCSC Ensembl
chr1:179819208..179819410hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6539230
Supporting Variants
Samples
Known GenesTOR1AIP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248833
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00118


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