A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683326



Internal ID21205187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79151528..79151528hg38UCSC Ensembl
chr17:77147610..77147610hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798266
Supporting Variants
Samples
Known GenesRBFOX3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683326
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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