A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2802181



Internal ID21247519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:28828651..28829043hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38393
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13690927
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2802181
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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