A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611648



Internal ID6651866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167129458..167130867hg38UCSC Ensembl
Innerchr6:167129502..167130823hg38UCSC Ensembl
Outerchr6:167129414..167130911hg38UCSC Ensembl
chr6:167542946..167544355hg19UCSC Ensembl
Innerchr6:167542990..167544311hg19UCSC Ensembl
Outerchr6:167542902..167544399hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381410
hg191410
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12640861, essv12640806, essv12640884, essv12640855, essv12640818, essv12640843, essv12640815, essv12640820, essv12640800, essv12640824, essv12640849, essv12640887, essv12640809, essv12640821, essv12640831, essv12640825, essv12640832, essv12640847, essv12640875, essv12640886, essv12640827, essv12640808, essv12640871, essv12640838, essv12640803, essv12640823, essv12640858, essv12640863, essv12640879, essv12640889, essv12640804, essv12640857, essv12640869, essv12640870, essv12640833, essv12640859, essv12640817, essv12640883, essv12640816, essv12640868, essv12640862, essv12640822, essv12640880, essv12640802, essv12640844, essv12640829, essv12640841, essv12640852, essv12640874, essv12640826, essv12640885, essv12640848, essv12640878, essv12640807, essv12640851, essv12640856, essv12640842, essv12640813, essv12640801, essv12640814, essv12640835, essv12640845, essv12640872, essv12640805, essv12640882, essv12640865, essv12640839, essv12640866, essv12640877, essv12640860, essv12640888, essv12640811, essv12640812, essv12640834, essv12640876, essv12640837, essv12640873, essv12640819, essv12640881, essv12640853, essv12640828, essv12640836, essv12640864, essv12640840, essv12640867, essv12640854, essv12640850, essv12640810, essv12640846, essv12640830
SamplesNA19445, HG02882, HG02108, HG03567, HG03279, HG02621, HG03351, NA19404, NA19437, NA19114, NA18874, NA19401, HG03055, HG03129, NA19023, NA18511, NA19223, HG02006, HG01085, NA18877, HG02952, HG03046, HG03571, HG01883, HG02010, NA19920, HG03103, NA19017, NA19236, NA19467, NA19143, HG02895, NA19117, NA20412, HG03558, NA19982, NA19984, HG03484, HG02568, HG02012, HG02667, NA18876, NA19351, NA19429, NA18916, HG03027, HG02595, HG02756, NA19042, NA19247, HG03126, NA19129, NA19393, HG01989, NA18498, NA19027, NA18486, NA19238, HG02594, NA19657, NA19098, NA18504, NA19175, NA19909, HG03157, HG02307, NA18910, NA19307, HG03115, NA19141, HG03175, HG02484, HG02281, NA18907, HG02923, NA19201, HG03061, NA19116, HG03367, HG03081, NA19327, HG02702, HG02891, HG03077, HG03449, HG02642, NA19113, NA19350, NA18908, NA19121
Known GenesCCR6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611648
Frequency
Sample Size2504
Observed Gain0
Observed Loss90
Observed Complex0
Frequencyn/a


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