A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451349



Internal ID21108902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66145401..66158600hg38UCSC Ensembl
chr9:42362730..42375865hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3813200
hg1913136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7810n223
Supporting Variantsnssv18217260
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451349
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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