A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636334



Internal ID7023128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45227371..45229137hg38UCSC Ensembl
Innerchr15:45227372..45229137hg38UCSC Ensembl
Outerchr15:45227371..45229138hg38UCSC Ensembl
chr15:45519569..45521335hg19UCSC Ensembl
Innerchr15:45519570..45521335hg19UCSC Ensembl
Outerchr15:45519569..45521336hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg381767
hg191767
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15233793, essv15233791, essv15233805, essv15233817, essv15233825, essv15233801, essv15233766, essv15233823, essv15233794, essv15233822, essv15233748, essv15233792, essv15233754, essv15233757, essv15233756, essv15233821, essv15233771, essv15233738, essv15233818, essv15233740, essv15233819, essv15233815, essv15233803, essv15233730, essv15233797, essv15233764, essv15233788, essv15233743, essv15233732, essv15233786, essv15233744, essv15233762, essv15233783, essv15233734, essv15233800, essv15233781, essv15233784, essv15233778, essv15233799, essv15233773, essv15233827, essv15233806, essv15233790, essv15233772, essv15233751, essv15233742, essv15233795, essv15233774, essv15233808, essv15233760, essv15233828, essv15233769, essv15233759, essv15233782, essv15233814, essv15233811, essv15233804, essv15233787, essv15233816, essv15233753, essv15233735, essv15233765, essv15233747, essv15233810, essv15233758, essv15233796, essv15233737, essv15233802, essv15233813, essv15233755, essv15233739, essv15233777, essv15233761, essv15233752, essv15233820, essv15233809, essv15233763, essv15233767, essv15233731, essv15233826, essv15233824, essv15233745, essv15233741, essv15233770, essv15233779, essv15233736, essv15233807, essv15233768, essv15233780, essv15233750, essv15233785, essv15233746, essv15233749, essv15233798, essv15233775, essv15233733, essv15233776, essv15233789, essv15233812
SamplesNA18502, HG03096, HG02339, NA19028, NA19141, NA19914, HG03175, HG02318, NA18917, HG03130, NA19092, HG02323, HG02476, NA19355, NA19819, HG03295, HG03515, HG03297, HG03193, HG03172, NA20356, HG03464, HG03099, NA20320, HG01167, NA18923, NA18498, NA19130, HG02143, HG03460, NA18874, NA19917, NA19137, NA19317, NA19159, NA20412, NA19209, NA20318, HG03270, HG03048, HG03120, HG02977, HG03160, HG03511, NA19175, NA19152, NA18933, HG01989, HG03575, NA20126, NA18871, HG02976, HG03472, NA18879, HG03382, HG03397, HG01241, NA18912, HG02309, HG03571, HG03451, NA19095, HG02635, HG01956, HG01990, NA19436, HG02772, NA19206, HG03028, NA19440, HG02282, HG02557, NA19256, NA19147, NA19712, NA19434, HG02546, HG02308, NA18865, HG03127, HG02941, NA19428, HG01108, NA18501, HG02971, NA19223, NA20334, NA19093, HG03063, NA20289, NA19185, NA18876, NA19711, NA19129, NA19316, HG01886, HG03198, HG03118, HG03166
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636334
Frequency
Sample Size2504
Observed Gain0
Observed Loss99
Observed Complex0
Frequencyn/a


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