A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671855



Internal ID2904942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23057052..23057455hg38UCSC Ensembl
chr8:22914565..22914968hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6195437, essv5630454, essv5806370, essv6326170, essv6232438, essv5851060, essv6289210, essv6098772, essv5469116, essv6053021
SamplesNA18523, NA19331, NA19324, NA19313, NA19393, NA18486, NA20334, NA18510, NA19901, NA19394
Known GenesTNFRSF10B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671855
Frequency
Sample Size1151
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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