A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13710402



Internal ID21232169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:98214199..98214268hg38UCSC Ensembl
chr9:100976481..100976550hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2820034
Supporting Variants
Samples
Known GenesTBC1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13710402
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.822581


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