A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442398



Internal ID21099951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66147801..66202700hg38UCSC Ensembl
chr9:42318543..42373464hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3854900
hg1954922
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7811n223
Supporting Variantsnssv18219229
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442398
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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