A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17026829



Internal ID85606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96726130..96726210hg38UCSC Ensembl
chr9:99488412..99488492hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492130
Supporting Variants
Samples
Known GenesLOC441455
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17026829
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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