A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696176



Internal ID21218027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:17143737..17143793hg38UCSC Ensembl
chr16:17237594..17237650hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794720
Supporting Variants
Samples
Known GenesXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696176
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.484375


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