A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260569



Internal ID20827609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183880868..183882057hg38UCSC Ensembl
chr3:183598656..183599845hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381190
hg191190
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6563993
Supporting Variants
Samples
Known GenesPARL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260569
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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