A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13695768



Internal ID21217620
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 StatusS
Merged Variantsnsv2806239
Supporting Variants
Samples
Known GenesTRAPPC12
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13695768
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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