A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657939



Internal ID9577358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:33374063..33376307hg38UCSC Ensembl
Outerchr8:33374026..33376357hg38UCSC Ensembl
Innerchr8:33231581..33233825hg19UCSC Ensembl
Outerchr8:33231544..33233875hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg382332
hg192332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5921295
SamplesNA20589
Known GenesFUT10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657939
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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