A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv861e214



Internal ID20122284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:2304094..2364791hg38UCSC Ensembl
chr3:2345778..2406475hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3860698
hg1960698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595026, esv3595025
SamplesNA12058, NA18873
Known GenesCNTN4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv861e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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