A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264979



Internal ID20832019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:26374585..26375033hg38UCSC Ensembl
chr4:26376207..26376655hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38449
hg19449
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6572868
Supporting Variants
Samples
Known GenesRBPJ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264979
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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