A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv455e199



Internal ID6311559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66706536..66706705hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
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
Method
Analysis
Platform
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv455e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss148
Observed Complex0
Frequencyn/a


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