A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234774



Internal ID20801814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34163276..34181693hg38UCSC Ensembl
chr9:34163274..34181691hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3818418
hg1918418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444843
Supporting Variants
Samples
Known GenesUBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234774
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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