A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv655e59



Internal ID22761875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62143053..62143196hg38UCSC Ensembl
chr11:61910525..61910668hg19UCSC Ensembl
chr11:61667101..61667244hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38144
hg19144
hg18144
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3302686, esv3302750
SamplesNA11995, NA18592, NA18508, NA10851, NA12414, NA11931, NA18603, NA12751, NA18545, NA07357, NA07346, NA19005, NA18944, NA18550, NA18519, NA18916, NA19138, NA19238, NA12044, NA19239, NA18605, NA12489, NA12003, NA18956, NA18948, NA18573, NA11894, NA12249, NA18570, NA18858, NA18593, NA19108, NA19240, NA07037, NA06986
Known GenesINCENP
MethodSequencing
Analysis
PlatformIllumina
Comments
Reference1000_Genomes_Consortium_Pilot_Project
Pubmed ID20981092
Accession Number(s)dgv655e59
Frequency
Sample Size185
Observed Gain35
Observed Loss0
Observed Complex0
Frequencyn/a


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