A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678627



Internal ID21200482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113745334..113745392hg38UCSC Ensembl
chr13:114448307..114448365hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792230
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678627
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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