A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv67e199



Internal ID20123369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:147188956..147198583hg38UCSC Ensembl
chr1:146660536..146670162hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg389628
hg199627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2674126, esv2664905
SamplesNA19819
Known GenesFMO5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv67e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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