A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2351e59



Internal ID20129100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224918091..224919889hg38UCSC Ensembl
chr2:225782808..225784606hg19UCSC Ensembl
chr2:225491052..225492850hg18UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg381799
hg191799
hg181799
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3342293, esv3332487, esv3407024
SamplesNA19239, NA19238, NA19240
Known GenesDOCK10
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2351e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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