A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663770



Internal ID9583189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:129481145..129487855hg38UCSC Ensembl
Outerchr10:129481108..129487905hg38UCSC Ensembl
Innerchr10:131279409..131286119hg19UCSC Ensembl
Outerchr10:131279372..131286169hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386798
hg196798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv174e199
Supporting Variantsessv5677914
SamplesHG01051
Known GenesMGMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663770
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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