A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670298



Internal ID9936403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103254862..103256360hg38UCSC Ensembl
Outerchr14:103254705..103256513hg38UCSC Ensembl
Innerchr14:103721199..103722697hg19UCSC Ensembl
Outerchr14:103721042..103722850hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381809
hg191809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5773421
SamplesNA19457
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670298
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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