A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv455e199



Internal ID20123757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66414198..66414367hg38UCSC Ensembl
chr15:66706536..66706705hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2675033, esv2657314
SamplesNA11830, NA18924, NA19909, NA11829, NA18592, NA10851, HG00100, NA11931, HG01374, HG01066, HG00306, NA18999, NA20512, NA12045, HG00318, NA18486, NA19819, NA18596, NA18959, HG00737, HG01518, HG01051, HG00261, NA12399, NA12155, HG01522, NA12341, HG00327, NA18967, HG01250, NA19660, NA19005, NA18944, NA18489, HG01351, NA19723, NA12891, NA12348, HG01492, NA07048, NA19054, HG00270, NA19782, HG00120, HG00148, HG00106, HG00156, NA20812, HG01495, NA19719, NA19372, HG00422, NA12889, NA20811, NA19189, HG01198, HG00159, NA19239, HG01048, HG01133, NA20342, HG00178, NA18867, HG00253, NA20515, NA19921, HG00264, NA11831, HG00543, HG00313, HG01136, HG00154, NA19908, NA12489, HG00266, HG01187, HG00145, HG00328, NA12878, NA20810, NA20536, HG00533, HG00263, HG00275, NA18579, NA20519, NA18630, NA18907, NA18537, HG01390, NA20525, NA18566, NA11919, HG00651, NA12249, NA19750, NA12892, HG00613, NA19009, NA18555, HG00146, HG00704, NA19225, NA12778, HG00126, HG01204, NA19012, NA18576, NA12043, NA18953, NA19003, HG00258, NA20799, NA18542, NA20801, NA18533, NA12716, NA19749, HG00366, HG00357, NA18941, HG00098, HG01375, NA19835, HG00607, HG00116, NA20803, NA20797, NA18610, NA12347, NA20341, HG01491, HG00312, NA20582, HG00267, HG01254, NA20510, NA18873, NA11843, NA18983, NA07056, HG01111, NA19758, NA18624, NA19463, NA07000, NA12154, NA12776
Known GenesMAP2K1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv455e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss148
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer