A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4134e59



Internal ID20130883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40819821..40821274hg38UCSC Ensembl
chr8:40677340..40678793hg19UCSC Ensembl
chr8:40796497..40797950hg18UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg381454
hg191454
hg181454
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3345865, esv3324588, esv3418343
SamplesNA19239, NA19240
Known GenesZMAT4
MethodSequencing
Analysis
PlatformIllumina
SOLiD
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv4134e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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