A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1398e59



Internal ID22762618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:28660365..28664363hg38UCSC Ensembl
chr15:28905511..28909509hg19UCSC Ensembl
chr15:26704552..26708550hg18UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg383999
hg193999
hg183999
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3362876, esv3428998
SamplesNA19238, NA19240
Known GenesHERC2P9
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1398e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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