A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449444



Internal ID21106997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66145201..66203500hg38UCSC Ensembl
chr9:42317743..42376065hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3858300
hg1958323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7811n223
Supporting Variantsnssv18225761
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449444
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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