A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220361



Internal ID20787401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96847801..96859000hg38UCSC Ensembl
chr9:99610083..99621282hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3811200
hg1911200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445691
Supporting Variants
Samples
Known GenesZNF782
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00036


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