A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478124



Internal ID255689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97911064..97911778hg38UCSC Ensembl
chr9:100673346..100674060hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38715
hg19715
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17026858
Samples
Known GenesC9orf156
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478124
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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