A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556662



Internal ID329794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121889036..121889256hg38UCSC Ensembl
chr9:124651315..124651535hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027958
Samples
Known GenesTTLL11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556662
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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