A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5921295



Internal ID8898698
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 Flag1
Merged StatusS
Merged Variantsesv2657939
Supporting Variants
SamplesNA20589
Known GenesFUT10
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5921295
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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