A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18228609



Internal ID20795649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66146401..66151400hg38UCSC Ensembl
chr9:42369869..42374865hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg385000
hg194997
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452035
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18228609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0011


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