A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027661



Internal ID86145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118692115..118692166hg38UCSC Ensembl
chr9:121454393..121454444hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg383341
hg193341
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556773
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027661
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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