A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662007



Internal ID9928112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121010188..121027998hg38UCSC Ensembl
chr10:122769701..122787511hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3817811
hg1917811
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv171e199
Supporting Variantsessv5864079, essv6185521, essv6578995, essv6290577, essv6032884, essv5988291, essv6198878, essv5961378, essv5589642, essv5450139, essv5559131, essv6468740, essv5926347, essv5573170, essv5958872, essv6300394, essv6149024, essv6416641, essv5491634, essv6055870, essv6248101, essv5484523, essv6417197, essv5637142, essv5992452, essv6111334, essv6010755, essv6436881, essv5803341, essv5445279, essv5805758, essv5732616
SamplesNA19394, NA19700, NA18870, NA18916, NA18874, NA19901, NA18867, NA19451, NA19247, NA19707, NA19403, NA19391, NA18516, NA19449, HG01101, NA18853, NA19099, NA19338, NA19257, NA19452, NA18909, NA19108, NA19256, NA19712, NA19434, HG00638, NA19835, NA19467, NA19818, NA19102, NA19429, NA18487
Known GenesMIR5694
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662007
Frequency
Sample Size1151
Observed Gain0
Observed Loss32
Observed Complex0
Frequencyn/a


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