A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv870e214



Internal ID22756764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:13577108..13679552hg38UCSC Ensembl
chr3:13618608..13721051hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38102445
hg19102444
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3595350, esv3595349
SamplesHG03490, HG03989
Known GenesFBLN2, LINC00620
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv870e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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