A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687607



Internal ID21209463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58710653..58710738hg38UCSC Ensembl
chr16:58744557..58744642hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795935
Supporting Variants
Samples
Known GenesGOT2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687607
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.59375


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