A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682686



Internal ID21204544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:55621512..55621512hg38UCSC Ensembl
chr18:53288743..53288743hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798475
Supporting Variants
Samples
Known GenesTCF4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682686
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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