A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706490



Internal ID21228283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32504871..32504871hg38UCSC Ensembl
chr9:32504869..32504869hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817840
Supporting Variants
Samples
Known GenesDDX58
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706490
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.15625


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