A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445609



Internal ID21103162
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 StatusM
Merged Variantsdgv7813n223
Supporting Variantsnssv18223527
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445609
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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