A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2806239



Internal ID21251577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3438040..3438040hg38UCSC Ensembl
chr2:3441811..3441811hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695768
Samples
Known GenesTRAPPC12
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2806239
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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