A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260566



Internal ID20827606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183859013..183859638hg38UCSC Ensembl
chr3:183576801..183577426hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568575
Supporting Variants
Samples
Known GenesPARL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260566
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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