A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450733



Internal ID21108286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40801301..41078800hg38UCSC Ensembl
chr9:66754329..69151904hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38277500
hg192397576
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7710n223
Supporting Variantsnssv18225535
Samples
Known GenesANKRD20A1, ANKRD20A3, AQP7P1, FAM27B, FAM27E3, LOC100132352, LOC286297, LOC642236, PGM5P2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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