A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13677014



Internal ID21198863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108991550..108991550hg38UCSC Ensembl
chr13:109643898..109643898hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793024
Supporting Variants
Samples
Known GenesMYO16
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13677014
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.921875


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