A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv890e214



Internal ID20122313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:49882736..49888371hg38UCSC Ensembl
chr3:49920169..49925804hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg385636
hg195636
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3596132, esv3596131
SamplesNA20527
Known GenesMST1R
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv890e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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