A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3676e59



Internal ID22764896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150332623..150333821hg38UCSC Ensembl
chr6:150653759..150654957hg19UCSC Ensembl
chr6:150695452..150696650hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381199
hg191199
hg181199
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3410509, esv3337133, esv3448259
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv3676e59
Frequency
Sample Size185
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer