A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13693579



Internal ID21215429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:37572215..37572265hg38UCSC Ensembl
chr20:36200617..36200667hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802926
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13693579
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.359375


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