A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431498



Internal ID21089051
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 StatusM
Merged Variants
Supporting Variantsnssv18225762
Samples
Known GenesIFNA22P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431498
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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