A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666548



Internal ID9585967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86196815..86197228hg38UCSC Ensembl
chr10:87956572..87956985hg19UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg38414
hg19414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5775430, essv6426593, essv5701724, essv6005351
SamplesHG00323, HG00269, HG00281, HG00361
Known GenesGRID1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666548
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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