A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709042



Internal ID21230822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:191390412..191390412hg38UCSC Ensembl
chr3:191108201..191108201hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807878
Supporting Variants
Samples
Known GenesCCDC50
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709042
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.8125


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