A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706471



Internal ID21228267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86694051..86694100hg38UCSC Ensembl
chr8:87706279..87706328hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818620
Supporting Variants
Samples
Known GenesCNGB3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706471
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.4


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