A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225762



Internal ID20792802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21257945..21280549hg38UCSC Ensembl
chr9:21257944..21280548hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3822605
hg1922605
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431498
Supporting Variants
Samples
Known GenesIFNA22P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225762
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00168


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