A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260257



Internal ID20827297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132678661..132679191hg38UCSC Ensembl
chr3:132397505..132398035hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559124
Supporting Variants
Samples
Known GenesNPHP3-ACAD11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260257
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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