A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1377e59



Internal ID22762597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22532087..22552585hg38UCSC Ensembl
chr15:23320511..23341009hg19UCSC Ensembl
chr15:20871952..20892450hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3820499
hg1920499
hg1820499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3449890, esv3429800
SamplesNA19238, NA19239
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1377e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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