A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17021579



Internal ID82033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15782634..15788701hg38UCSC Ensembl
chr9:15782632..15788699hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg386068
hg196068
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555019
Supporting Variants
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17021579
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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