A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1391e59



Internal ID22762611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28311011..28312709hg38UCSC Ensembl
chr15:28556157..28557855hg19UCSC Ensembl
chr15:26229752..26231450hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg381699
hg191699
hg181699
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3344745, esv3350263, esv3409154
SamplesNA19238, NA19239, NA19240
Known GenesHERC2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1391e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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