A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683164



Internal ID21205021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:78659304..78659304hg38UCSC Ensembl
chr13:79233439..79233439hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38206
hg19206
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794004
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683164
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.76087


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