A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025697



Internal ID84866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93323455..93367118hg38UCSC Ensembl
chr9:96085737..96129400hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg3843664
hg1943664
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554929
Supporting Variants
Samples
Known GenesC9orf129
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025697
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.025601


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