A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682784



Internal ID21204641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:48897114..48897177hg38UCSC Ensembl
chr20:47513651..47513714hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682784
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.166667


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