A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696164



Internal ID21218015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37337986..37338195hg38UCSC Ensembl
chr18:34917949..34918158hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798757
Supporting Variants
Samples
Known GenesCELF4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696164
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.96875


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