A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027725



Internal ID86186
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 StatusS
Merged Variantsnsv5559125
Supporting Variants
Samples
Known GenesTTLL11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027725
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.004374


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