A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18259645



Internal ID20826685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:130745783..130747412hg38UCSC Ensembl
chr3:130464627..130466256hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg381630
hg191630
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571351
Supporting Variants
Samples
Known GenesPIK3R4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18259645
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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