A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233124



Internal ID20800164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:125769645..125801934hg38UCSC Ensembl
chr9:128531924..128564213hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3832290
hg1932290
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441951
Supporting Variants
Samples
Known GenesPBX3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233124
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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