A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688902



Internal ID21210754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110252459..110252514hg38UCSC Ensembl
chr13:110904806..110904861hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793261
Supporting Variants
Samples
Known GenesCOL4A1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688902
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.609375


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