A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18233384



Internal ID20800424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133129998..133132748hg38UCSC Ensembl
chr9:136005385..136008135hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg382751
hg192751
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6436211
Supporting Variants
Samples
Known GenesRALGDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18233384
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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