A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231219



Internal ID20798259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19262015..19401585hg38UCSC Ensembl
chr9:19262013..19401583hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg38139571
hg19139571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429305
Supporting Variants
Samples
Known GenesDENND4C, RPS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231219
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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