A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681025



Internal ID21202888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:34374248..34374248hg38UCSC Ensembl
chr14:34843454..34843454hg19UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681025
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0625


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