A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559125



Internal ID332169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121902098..121902137hg38UCSC Ensembl
chr9:124664377..124664416hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV sva insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027725
Samples
Known GenesTTLL11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559125
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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