A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660949



Internal ID9927054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1405079..1405331hg38UCSC Ensembl
Outerchr19:1405042..1405381hg38UCSC Ensembl
Innerchr19:1405078..1405330hg19UCSC Ensembl
Outerchr19:1405041..1405380hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5697990, essv5462546
SamplesNA18555, NA18593
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660949
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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