A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556060



Internal ID329205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69370981..69372260hg38UCSC Ensembl
chr9:71985897..71987176hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg381280
hg191280
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17023222
Samples
Known GenesFAM189A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556060
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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