A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223928



Internal ID20790968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66147201..66152400hg38UCSC Ensembl
chr9:42368869..42374065hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg385200
hg195197
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6447205
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223928
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00074


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