A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18224764



Internal ID20791804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128761730..128795415hg38UCSC Ensembl
chr9:131524009..131557694hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3833686
hg1933686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438017
Supporting Variants
Samples
Known GenesTBC1D13, ZER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18224764
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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