A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679669



Internal ID21201527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:64012575..64012575hg38UCSC Ensembl
chr20:62643928..62643928hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803173
Supporting Variants
Samples
Known GenesPRPF6
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679669
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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