A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704183



Internal ID21225952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55687191..55687191hg38UCSC Ensembl
chr16:55721103..55721103hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796035
Supporting Variants
Samples
Known GenesSLC6A2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704183
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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