A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2807241



Internal ID21252579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238398011..238398011hg38UCSC Ensembl
chr2:239306652..239306652hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689546
Samples
Known GenesTRAF3IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2807241
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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