A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027586



Internal ID86096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97815629..97815664hg38UCSC Ensembl
chr9:100577911..100577946hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5550238
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027586
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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