A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635760



Internal ID6675871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22048953..22056013hg38UCSC Ensembl
chr15:22336904..22343964hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg387061
hg197061
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv434e214
Supporting Variantsessv15156901, essv15156860, essv15156950, essv15156878, essv15156882, essv15156893, essv15156939, essv15156875, essv15156912, essv15156870, essv15156853, essv15156922, essv15156888, essv15156916, essv15156900, essv15156845, essv15156921, essv15156861, essv15156895, essv15156848, essv15156943, essv15156867, essv15156877, essv15156913, essv15156927, essv15156865, essv15156934, essv15156929, essv15156904, essv15156876, essv15156864, essv15156920, essv15156847, essv15156914, essv15156949, essv15156884, essv15156937, essv15156846, essv15156928, essv15156859, essv15156881, essv15156947, essv15156938, essv15156896, essv15156880, essv15156907, essv15156930, essv15156869, essv15156911, essv15156931, essv15156915, essv15156897, essv15156948, essv15156891, essv15156856, essv15156905, essv15156863, essv15156885, essv15156919, essv15156883, essv15156942, essv15156925, essv15156946, essv15156871, essv15156866, essv15156941, essv15156935, essv15156940, essv15156933, essv15156953, essv15156906, essv15156855, essv15156909, essv15156902, essv15156849, essv15156879, essv15156892, essv15156889, essv15156868, essv15156851, essv15156874, essv15156858, essv15156862, essv15156890, essv15156898, essv15156872, essv15156857, essv15156926, essv15156908, essv15156910, essv15156854, essv15156918, essv15156903, essv15156886, essv15156887, essv15156952, essv15156923, essv15156924, essv15156852, essv15156945, essv15156932, essv15156936, essv15156899, essv15156850, essv15156873, essv15156843, essv15156844, essv15156917, essv15156944, essv15156951, essv15156894
SamplesNA19701, HG02339, NA20339, NA19028, NA19141, NA19222, HG02944, NA19700, NA18924, NA19204, NA18508, HG03163, HG04222, HG03175, NA18881, HG03449, NA18639, HG03298, NA19393, HG03193, NA19098, NA20359, NA18510, NA19107, HG03199, NA19446, HG03436, NA19201, HG02811, HG03135, HG03452, HG02840, NA19457, HG02922, HG03079, HG02489, HG02143, HG02573, NA18868, HG03212, NA19372, NA19235, NA19207, HG02420, HG02571, HG02946, NA19209, HG02623, NA19921, HG02442, HG03160, HG03132, NA19462, NA19152, NA18933, HG03547, NA19184, NA19913, HG02554, NA20126, HG02968, HG03294, HG03123, NA19461, HG03078, HG02008, HG03446, NA19320, HG01890, HG00704, HG02586, HG01988, NA18858, HG01956, NA19035, HG03567, NA19401, HG03240, HG01362, NA19037, NA19439, HG02814, HG02558, NA18501, HG02379, HG02095, NA19438, HG03279, HG01846, HG02107, NA19093, HG03060, HG03258, NA20289, NA18873, NA18876, NA19116, NA19711, HG03445, HG02947, NA18488, HG02465, NA18968, NA18522, HG02808, HG03129, HG00180, HG03439, NA19153, HG03271, HG02760
Known GenesLOC727924
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635760
Frequency
Sample Size2504
Observed Gain111
Observed Loss0
Observed Complex0
Frequencyn/a


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