A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678799



Internal ID21200655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31723080..31723080hg38UCSC Ensembl
chr13:32297217..32297217hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793778
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678799
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03125


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