A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685280



Internal ID21207140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:18507489..18507489hg38UCSC Ensembl
chr16:14982393..14982393hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794725
Supporting Variants
Samples
Known GenesNOMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685280
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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