A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264603



Internal ID20831643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40807471..40808026hg38UCSC Ensembl
chr4:40809488..40810043hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6566455
Supporting Variants
Samples
Known GenesNSUN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264603
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00031


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