A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659963



Internal ID9926068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:77349143..77351256hg38UCSC Ensembl
Outerchr14:77349106..77351306hg38UCSC Ensembl
Innerchr14:77815486..77817599hg19UCSC Ensembl
Outerchr14:77815449..77817649hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5935646
SamplesNA19081
Known GenesTMED8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659963
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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