A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026901



Internal ID85657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100151532..100151582hg38UCSC Ensembl
chr9:102913814..102913864hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474446
Supporting Variants
Samples
Known GenesINVS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026901
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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