A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3087e59



Internal ID22764307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:140286748..140290246hg38UCSC Ensembl
chr4:141207902..141211400hg19UCSC Ensembl
chr4:141427352..141430850hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg383499
hg193499
hg183499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3378966, esv3352205, esv3447879
SamplesNA19238, NA19239, NA19240
Known GenesLOC100129858, SCOC
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3087e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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