A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026858



Internal ID85626
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 StatusS
Merged Variantsnsv5478124
Supporting Variants
Samples
Known GenesC9orf156
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026858
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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