A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264778



Internal ID20831818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:145175706..145176423hg38UCSC Ensembl
chr4:146096858..146097575hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38718
hg19718
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560012
Supporting Variants
Samples
Known GenesOTUD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264778
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00029


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