A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662654



Internal ID9582073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78459168..78459523hg38UCSC Ensembl
chr11:78170214..78170569hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5574209, essv5858648, essv5662256, essv6528442, essv5596524, essv6550037, essv5495726, essv6175056, essv5651412, essv5762538, essv5928676, essv6143137, essv5884821, essv6562984, essv5450937, essv5964562
SamplesNA19700, HG01051, HG01250, NA19315, NA18498, NA20278, NA18867, NA19451, NA19982, NA18853, NA19401, NA19834, NA19712, NA19398, NA19213, NA19431
Known GenesNARS2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662654
Frequency
Sample Size1151
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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