A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558918



Internal ID331968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:14375421..14376816hg38UCSC Ensembl
chr9:14375420..14376815hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg381396
hg191396
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17019089
Samples
Known GenesNFIB
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558918
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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