A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217415



Internal ID20784455
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 StatusS
Merged Variantsnsv6443841
Supporting Variants
Samples
Known GenesTMEM2, TRPM3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217415
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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