A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687538



Internal ID21209393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65965604..65965604hg38UCSC Ensembl
chr15:66257942..66257942hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794981
Supporting Variants
Samples
Known GenesMEGF11
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687538
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.211538


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