A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv455e199

Internal ID18982509
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66414198..66414367hg38UCSC Ensembl
chr15:66706536..66706705hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2657314, esv2675033
SamplesHG00613, NA19012, NA12154, HG00313, NA12043, NA12489, HG01518, NA12249, HG00318, HG00607, HG01250, NA18630, HG00100, NA19819, HG00328, HG00145, NA07056, NA20510, NA12347, NA19003, HG00261, NA11931, HG01051, HG01492, NA18953, NA20342, HG01491, HG00148, NA18542, NA19782, HG00270, NA18489, HG00106, HG01204, NA12776, HG00651, HG00366, HG00146, HG00737, HG00253, NA12341, NA20803, HG00156, NA18873, NA18596, HG01133, HG00266, HG00543, HG00154, HG01254, NA19463, NA11919, NA18624, NA18967, NA19054, NA19239, NA20515, HG01375, NA18566, NA20811, NA19660, NA12155, NA18576, HG01048, HG01495, NA20801, NA18592, NA07048, NA19908, HG00098, NA18959, HG00533, HG00178, HG00258, NA11843, NA11831, HG01136, NA19835, HG00264, HG01187, HG00357, NA20341, HG00306, HG00159, HG00267, HG01111, NA12716, NA18537, NA19189, NA12892, NA19372, NA20536, HG01066, NA20512, NA12778, NA12348, NA18486, HG00263, NA19005, NA18941, HG00116, HG01351, NA19909, NA20797, NA20582, NA18579, HG00120, NA12891, NA10851, NA18999, NA20525, NA19921, NA18983, NA18907, NA19723, NA20799, NA18867, NA19009, NA12889, NA19719, HG01390, NA12878, NA18533, NA11830, NA20810, NA19749, NA18944, NA19225, NA12399, NA20812, HG00422, NA18924, NA18610, NA12045, NA11829, HG00275, HG01374, HG01522, NA19758, HG00704, NA18555, NA19750, NA20519, HG00126, NA07000, HG00312, HG00327, HG01198
Known GenesMAP2K1
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)dgv455e199
Sample Size1151
Observed Gain0
Observed Loss148
Observed Complex0

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