A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585326



Internal ID6972850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16020256..16041292hg38UCSC Ensembl
chr1:16346751..16367787hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821037
hg1921037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10e214
Supporting Variantsessv9864812, essv9864765, essv9864838, essv9864853, essv9864843, essv9864847, essv9864792, essv9864841, essv9864829, essv9864769, essv9864806, essv9864839, essv9864775, essv9864763, essv9864825, essv9864842, essv9864779, essv9864778, essv9864788, essv9864820, essv9864776, essv9864833, essv9864822, essv9864791, essv9864770, essv9864831, essv9864817, essv9864807, essv9864777, essv9864801, essv9864790, essv9864784, essv9864768, essv9864821, essv9864861, essv9864832, essv9864762, essv9864816, essv9864799, essv9864846, essv9864863, essv9864767, essv9864805, essv9864827, essv9864804, essv9864796, essv9864836, essv9864782, essv9864865, essv9864819, essv9864761, essv9864781, essv9864798, essv9864814, essv9864759, essv9864815, essv9864823, essv9864787, essv9864837, essv9864828, essv9864771, essv9864772, essv9864810, essv9864813, essv9864794, essv9864852, essv9864851, essv9864859, essv9864800, essv9864824, essv9864785, essv9864849, essv9864834, essv9864793, essv9864844, essv9864809, essv9864797, essv9864786, essv9864774, essv9864802, essv9864795, essv9864758, essv9864845, essv9864835, essv9864818, essv9864864, essv9864773, essv9864856, essv9864760, essv9864862, essv9864860, essv9864808, essv9864766, essv9864855, essv9864840, essv9864857, essv9864764, essv9864858, essv9864826, essv9864789, essv9864850, essv9864803, essv9864783, essv9864811, essv9864848, essv9864780, essv9864854, essv9864830
SamplesHG01986, HG03096, HG03366, HG02496, HG03548, NA18508, HG01885, HG02433, HG02318, HG03300, HG02419, HG02012, NA20321, HG03521, NA18504, HG03518, NA19920, HG02769, HG03086, HG02811, HG03385, NA18489, HG02756, HG03370, HG02549, NA19023, HG01063, NA20291, NA19130, HG03189, HG02573, HG01170, NA19172, NA19159, HG03352, NA19901, HG03073, NA19209, HG02623, NA19456, HG03394, NA18867, HG02977, NA19247, HG03160, HG03132, HG02090, NA19347, NA19152, HG03547, NA18915, HG02450, HG03575, NA20126, HG03159, HG02976, HG02878, HG02537, HG02757, HG02555, HG03311, HG03563, HG03472, HG03301, NA19449, HG03136, NA18912, HG02884, HG02283, NA19338, HG02896, NA19625, NA18858, HG03109, NA19436, NA19035, HG03567, NA19401, HG02455, HG03028, HG02807, HG02667, NA18909, HG03240, NA19108, NA19712, NA19473, NA19454, HG02923, HG02982, NA19428, NA19310, HG01108, HG03108, NA19143, HG03097, HG03066, HG02646, HG02938, NA19093, NA18876, NA19213, NA19121, HG02861, HG03198, NA19429, NA19346, HG03166
Known GenesCLCNKA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585326
Frequency
Sample Size2504
Observed Gain108
Observed Loss0
Observed Complex0
Frequencyn/a


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