A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706298



Internal ID21228093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75067410..75067495hg38UCSC Ensembl
chr18:72779366..72779451hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798154
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706298
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.9375


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