A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264190



Internal ID20831230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:118819284..118820225hg38UCSC Ensembl
chr4:119740439..119741380hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg38942
hg19942
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6568798
Supporting Variants
Samples
Known GenesSEC24D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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