A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18248768



Internal ID20815808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175231430..175232801hg38UCSC Ensembl
chr1:175200566..175201937hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381372
hg191372
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554781
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18248768
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.46939


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