A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558541



Internal ID331600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97913251..97913251hg38UCSC Ensembl
chr9:100675533..100675533hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026859
Samples
Known GenesC9orf156
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558541
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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