A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv871e214



Internal ID22756765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14548209..14569831hg38UCSC Ensembl
chr3:14589716..14611338hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3821623
hg1921623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595369, esv3595370
SamplesHG01918, HG02266, HG02253, HG01921, NA19652, HG02308, HG01342, HG00595, NA19146
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv871e214
Frequency
Sample Size2504
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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