A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1218e214



Internal ID20122641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:127723211..127730024hg38UCSC Ensembl
chr6:128044356..128051169hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg386814
hg196814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3610727, esv3610729
SamplesNA18977, HG03419
Known GenesTHEMIS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1218e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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