A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677640



Internal ID9943745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96886630..96897397hg38UCSC Ensembl
Outerchr14:96886593..96897447hg38UCSC Ensembl
Innerchr14:97352967..97363734hg19UCSC Ensembl
Outerchr14:97352930..97363784hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3810855
hg1910855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv411e199
Supporting Variantsessv6227787, essv5438094
SamplesNA18597, NA18562
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677640
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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