A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261114



Internal ID20828154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165236468..165236919hg38UCSC Ensembl
chr3:164954256..164954707hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6561130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261114
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00026


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