A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489007



Internal ID266299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94901415..94904585hg38UCSC Ensembl
chr9:97663697..97666867hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg383171
hg193171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17025823
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489007
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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