A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1399e59



Internal ID22762619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:30375057..30376455hg38UCSC Ensembl
chr15:30667260..30668658hg19UCSC Ensembl
chr15:28454552..28455950hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg381399
hg191399
hg181399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3401885, esv3435221
SamplesNA19239, NA19240
Known GenesCHRFAM7A
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv1399e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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