A curated catalogue of human genomic structural variation
About the Project
Genome Browser
Downloads
Query Tool
Links
Submissions
Statistics
Contact Us
FAQ
Training Resources
Variant Details
Variant: dgv2610e59
Internal ID
20129359
Landmark
Location Information
Type
Coordinates
Assembly
Other Links
chr22:33565593..33565711
hg38
UCSC
Ensembl
chr22:33961579..33961697
hg19
UCSC
Ensembl
chr22:32291579..32291697
hg18
UCSC
Ensembl
Cytoband
22q12.3
Allele length
Assembly
Allele length
hg38
119
hg19
119
hg18
119
Variant Type
CNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged Status
M
Merged Variants
Supporting Variants
esv3303039
,
esv3302441
Samples
NA11995, NA18861, NA10851, NA12004, NA19005, NA12891, NA18547, NA18916, NA19138, NA12156, NA19238, NA12044, NA11993, NA18951, NA12878, NA18956, NA12892, NA18542, NA12749, NA12006, NA18965
Known Genes
LARGE
Method
Sequencing
Analysis
Platform
Illumina
Comments
Reference
1000_Genomes_Consortium_Pilot_Project
Pubmed ID
20981092
Accession Number(s)
dgv2610e59
Frequency
Sample Size
185
Observed Gain
21
Observed Loss
0
Observed Complex
0
Frequency
n/a
Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage
disclaimer