A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2678828



Internal ID9944933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:69471074..69478068hg38UCSC Ensembl
Outerchr10:69471037..69478118hg38UCSC Ensembl
Innerchr10:71230830..71237824hg19UCSC Ensembl
Outerchr10:71230793..71237874hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg387082
hg197082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5772856
SamplesHG01375
Known GenesTSPAN15
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2678828
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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