A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105198



Internal ID22014431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:121935054..121969172hg38UCSC Ensembl
chr5:121270749..121304867hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3834119
hg1934119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17541674
Samples
Known GenesSRFBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105198
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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