A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635761



Internal ID6675872
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 Variantsessv15157009, essv15157002, essv15156999, essv15157011, essv15156982, essv15156995, essv15156969, essv15156971, essv15157042, essv15157046, essv15156957, essv15157034, essv15157006, essv15157017, essv15157001, essv15157041, essv15156960, essv15157012, essv15157005, essv15157032, essv15156955, essv15156976, essv15156994, essv15157010, essv15156979, essv15156974, essv15157014, essv15157024, essv15157027, essv15157023, essv15156981, essv15156961, essv15157031, essv15156991, essv15156959, essv15156996, essv15156992, essv15157033, essv15157020, essv15157043, essv15157029, essv15156989, essv15157022, essv15157044, essv15156986, essv15156985, essv15157004, essv15157013, essv15157008, essv15156998, essv15156956, essv15156962, essv15156980, essv15156984, essv15156972, essv15156975, essv15156997, essv15156990, essv15157028, essv15157038, essv15156954, essv15157003, essv15157037, essv15157039, essv15156973, essv15157007, essv15157045, essv15157016, essv15157019, essv15156978, essv15156958, essv15156993, essv15156967, essv15157030, essv15157035, essv15156964, essv15157000, essv15157015, essv15157021, essv15157018, essv15157025, essv15156983, essv15157026, essv15156965, essv15156968, essv15156963, essv15156970, essv15156988, essv15156977, essv15157040, essv15156966, essv15156987, essv15157036
SamplesHG01412, HG03857, HG00592, HG01054, NA20891, NA19397, NA19399, HG02702, NA21100, HG03241, HG02804, HG03298, NA20298, HG03455, HG03518, HG03372, HG03168, HG02407, NA20890, HG02952, NA18942, HG03342, NA19197, NA18642, NA19384, HG02111, HG01242, HG02561, HG00632, HG01767, HG01673, HG02588, NA19189, HG03649, HG03394, HG03114, NA18973, HG04075, NA18638, HG03343, HG03780, NA19210, NA19437, HG01847, HG00282, HG03787, HG02142, HG01879, NA19982, HG02450, HG00320, NA18757, NA18907, HG03085, HG00684, NA18856, NA19001, HG00525, HG02601, HG02635, HG01811, NA18632, HG02667, NA19747, NA19019, HG00742, HG03458, HG03117, HG02923, NA20351, NA19380, NA19144, HG02982, HG02941, HG02464, NA07037, HG04003, HG01862, NA19078, HG00672, HG03157, HG00329, NA19713, HG02116, NA21101, NA20510, HG01872, NA19711, NA18983, HG03162, HG02343, HG01786, NA18620
Known GenesLOC727924
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635761
Frequency
Sample Size2504
Observed Gain93
Observed Loss0
Observed Complex0
Frequencyn/a


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