A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233609



Internal ID20800649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66146501..66202100hg38UCSC Ensembl
chr9:42319143..42374765hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3855600
hg1955623
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438651
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00326


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