A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18222054



Internal ID20789094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66146601..66152400hg38UCSC Ensembl
chr9:42368869..42374665hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg385800
hg195797
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453557
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18222054
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00108


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