A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223527



Internal ID20790567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66146601..66173800hg38UCSC Ensembl
chr9:42347549..42374665hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3827200
hg1927117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6445609
Supporting Variants
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223527
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00055


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