A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3706e59



Internal ID22764926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164925373..164926671hg38UCSC Ensembl
chr6:165338862..165340160hg19UCSC Ensembl
chr6:165258852..165260150hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3414452, esv3446736
SamplesNA19238, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3706e59
Frequency
Sample Size185
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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