A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793500



Internal ID21238838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18196941..18196941hg38UCSC Ensembl
chrUn_gl000212:25693..25693hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38173
hg19173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13685743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793500
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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