A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711113



Internal ID21232873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:4185399..4185682hg38UCSC Ensembl
chr20:4166046..4166329hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802239
Supporting Variants
Samples
Known GenesSMOX
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711113
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.59375


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