A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476151



Internal ID253769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87159176..87159409hg38UCSC Ensembl
chr9:89774091..89774324hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025432
Samples
Known GenesC9orf170
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476151
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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