A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264775



Internal ID20831815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145151412..145152228hg38UCSC Ensembl
chr4:146072564..146073380hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38817
hg19817
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6559613
Supporting Variants
Samples
Known GenesOTUD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264775
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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