A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219474



Internal ID20786514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66151701..66175300hg38UCSC Ensembl
chr9:42346062..42369568hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3823600
hg1923507
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448028
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219474
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00142


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