A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677780



Internal ID9943885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103182559..103185288hg38UCSC Ensembl
Outerchr14:103182402..103185452hg38UCSC Ensembl
Innerchr14:103648896..103651625hg19UCSC Ensembl
Outerchr14:103648739..103651789hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg383051
hg193051
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5676814
SamplesNA18908
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677780
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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