A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278871



Internal ID20488089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:40233387..40235438hg38UCSC Ensembl
chr4:40235007..40237058hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382052
hg192052
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4760594
Supporting Variants
Samples
Known GenesRHOH
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278871
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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