A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820034



Internal ID21265372
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 StatusM
Merged Variants
Supporting Variantsnssv13710402
Samples
Known GenesTBC1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820034
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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