A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673495



Internal ID9592914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129617859..129618771hg38UCSC Ensembl
chr10:131416123..131417035hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38913
hg19913
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5808283, essv6417012, essv5933920, essv6037522, essv6494352, essv5775851, essv6005174, essv5577918, essv5514149, essv6012788, essv5718311, essv5734751, essv5676882, essv6549155, essv5774229, essv5422768, essv6589980, essv5632741, essv6572061
SamplesHG00702, HG00369, HG00309, HG00530, HG00268, HG00282, HG00556, HG00275, HG00404, HG00476, HG00336, HG00353, HG00319, HG00578, HG00312, HG00656, HG00377, HG00180, HG00581
Known GenesMGMT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673495
Frequency
Sample Size1151
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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