A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5437873



Internal ID8948759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:23728806..23739552hg38UCSC Ensembl
Outerchr14:23728649..23739718hg38UCSC Ensembl
Innerchr14:24198015..24208761hg19UCSC Ensembl
Outerchr14:24197858..24208927hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3811070
hg1911070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665605
Supporting Variants
SamplesHG00479
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5437873
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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