A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv17e199



Internal ID20123319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15594114..15610810hg38UCSC Ensembl
chr1:15920609..15937305hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3816697
hg1916697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672627, esv2660595
SamplesNA19834
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv17e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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