A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680111



Internal ID21201976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:17653920..17653920hg38UCSC Ensembl
chr4:17655543..17655543hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809765
Supporting Variants
Samples
Known GenesFAM184B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680111
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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