A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3727e59



Internal ID22764947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170736739..170745937hg38UCSC Ensembl
chr6:171045827..171055000hg19UCSC Ensembl
chr6:170887752..170896950hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg389199
hg199174
hg189199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3325682, esv3327888, esv3352863, esv3410422, esv3381616, esv3434666
SamplesNA12891, NA19238, NA19239, NA12878, NA12892, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3727e59
Frequency
Sample Size185
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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