A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443841



Internal ID21101394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71101404..71757322hg38UCSC Ensembl
chr9:73716320..74372238hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg38655919
hg19655919
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7819n223
Supporting Variantsnssv18217415
Samples
Known GenesTMEM2, TRPM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443841
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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