A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027536



Internal ID86062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97123539..97123539hg38UCSC Ensembl
chr9:99885821..99885821hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5552964
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17027536
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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