A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669390



Internal ID9935495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131110795..131114516hg38UCSC Ensembl
chr10:132909058..132912779hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg383722
hg193722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv175e199
Supporting Variantsessv6312891, essv6530049, essv6493870, essv6294992, essv5449263, essv5848694, essv5972855, essv5804384, essv6351809, essv6149747, essv5641029, essv5984260, essv6272135, essv5973003, essv5791394, essv5620964, essv6329278, essv6516364, essv5699758, essv6288463, essv5898511, essv5406171, essv5546415, essv5727355, essv5614186, essv5404925, essv6519725, essv5494226, essv6043363, essv6497510, essv5441703, essv5569205, essv5905272, essv6509774, essv5699771, essv5422043, essv5603677, essv6007072, essv6212362, essv6074963, essv5797357, essv6597750, essv5886392, essv5589843, essv6571888, essv6445770, essv5400912, essv5782179, essv6183195, essv6214246, essv5941012, essv5557633, essv6059651, essv5418198, essv5924168, essv5605133, essv5658515, essv5840223, essv5652266, essv5962847, essv6511222, essv6533399, essv5640031, essv6319979, essv5847420, essv6154569
SamplesNA20588, HG00189, NA20761, NA20529, NA20783, HG00306, NA20816, HG00181, HG00177, NA20517, NA20507, HG00272, NA20586, NA20795, NA20768, NA20540, HG00270, HG00185, HG00311, NA20541, HG00281, HG00335, NA20819, NA20775, NA20812, HG00182, HG00326, HG00178, NA20515, NA20753, NA20818, HG00266, HG00282, NA20524, HG00328, NA20760, NA20536, HG00368, HG00320, HG00275, NA20506, HG00273, HG00373, NA20538, HG00321, NA20542, HG00285, HG00375, HG00357, NA20804, NA20520, NA20785, NA20527, HG00319, HG00312, HG00329, HG00342, HG00174, NA20510, HG00280, NA20758, NA20826, HG00377, HG00171, HG00345, NA20772
Known GenesTCERG1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669390
Frequency
Sample Size1151
Observed Gain0
Observed Loss66
Observed Complex0
Frequencyn/a


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