A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5572707



Internal ID9874249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:84465876..84466829hg38UCSC Ensembl
Outerchr14:84465839..84466879hg38UCSC Ensembl
Innerchr14:84932220..84933173hg19UCSC Ensembl
Outerchr14:84932183..84933223hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg381041
hg191041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2674435
Supporting Variants
SamplesNA20582
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5572707
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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