A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027557



Internal ID86076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97318864..97340961hg38UCSC Ensembl
chr9:100081146..100103243hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3822098
hg1922098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492948
Supporting Variants
Samples
Known GenesCCDC180, LOC100499484-C9ORF174
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027557
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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