A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806683



Internal ID21252022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:80494698..80494698hg38UCSC Ensembl
chr2:80721823..80721823hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13679768
Samples
Known GenesCTNNA2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806683
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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