A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260258



Internal ID20827298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132678795..132679247hg38UCSC Ensembl
chr3:132397639..132398091hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38453
hg19453
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6557474
Supporting Variants
Samples
Known GenesNPHP3-ACAD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260258
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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