A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668552



Internal ID9934657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:68391206..68395052hg38UCSC Ensembl
Outerchr14:68391169..68395102hg38UCSC Ensembl
Innerchr14:68857923..68861769hg19UCSC Ensembl
Outerchr14:68857886..68861819hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg383934
hg193934
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv399e199
Supporting Variantsessv6590946
SamplesHG00323
Known GenesRAD51B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668552
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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