A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2366e59



Internal ID22763586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237128370..237131968hg38UCSC Ensembl
chr2:238037013..238040611hg19UCSC Ensembl
chr2:237701752..237705350hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg383599
hg193599
hg183599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3337585, esv3434551, esv3400576
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv2366e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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