A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672004



Internal ID9938109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73191424..73191478hg38UCSC Ensembl
Outerchr15:73191267..73191631hg38UCSC Ensembl
Innerchr15:73483765..73483819hg19UCSC Ensembl
Outerchr15:73483608..73483972hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38365
hg19365
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5751489, essv6169763, essv6315895, essv6484420, essv5569787, essv6406834, essv6565625, essv6122535, essv6528379, essv6132127, essv5764183, essv6122674, essv6544485, essv6292367, essv5420708, essv5795845, essv5991195, essv5522545, essv6323813, essv5600296, essv5801684, essv5415658, essv5668087, essv6030637, essv5797238, essv6183721, essv5789486, essv6314268, essv6021846, essv6225311, essv5830974, essv6158774, essv6292646, essv6300067, essv6230899, essv5907000, essv6133106, essv6156722, essv5799904, essv5934533, essv5637548, essv6231487, essv6537502, essv5657336, essv5836398, essv6011633, essv5597753, essv6030121, essv5724521, essv5460550, essv5539335, essv5917683, essv5533117, essv5731431, essv5824718, essv5964004, essv6595742, essv5832504, essv6206530, essv6597842, essv6169030, essv5519933, essv5568078, essv5620985, essv6592485, essv6317707, essv5903645, essv5672187, essv5893328, essv5717420, essv5786265, essv6243723, essv5995963, essv6203792, essv6595972, essv6358190, essv6473921, essv5709196, essv6486834, essv6348568, essv6254364, essv6384747, essv5865921, essv6492280, essv6589301, essv6398375, essv5704324, essv6367200, essv5550209, essv6029282, essv6036882, essv6562224, essv6121566, essv6290925, essv6447944, essv5486961, essv5942702, essv5780429, essv6101513, essv5916995, essv5987366, essv6488681, essv5668114, essv5977693, essv5539733, essv5662078, essv6306135, essv6558132, essv6295340, essv5892545, essv5717997, essv5714566, essv5911402, essv6194429, essv5587918, essv5466675, essv6108049, essv5952194, essv6580467, essv6078118, essv5872923, essv5569093, essv5801236, essv6123061, essv6598008, essv6563607, essv6429948, essv6527473, essv5410936, essv6323696, essv5526456, essv5987865, essv5455444, essv6238441, essv5477247, essv6570212, essv5826321, essv6373069, essv6496250, essv5470608, essv5785531, essv6362064, essv5604144, essv6203652, essv5778781, essv6536031, essv5691185, essv5738587, essv5455871, essv5741166, essv5524767, essv5718494
SamplesNA20588, HG01060, HG01441, HG00650, HG01173, HG00536, HG00231, HG00671, HG00559, HG01052, HG01079, HG01188, HG01389, HG01374, HG01066, HG00315, HG00640, HG00318, NA12751, NA19393, NA18504, NA18530, HG00150, HG01140, HG00337, HG00327, HG00271, HG00663, HG00138, NA19381, NA19373, HG01350, HG01366, HG01070, HG00251, NA19382, HG01351, HG00702, HG00448, NA18982, HG00634, NA11918, NA18582, HG01365, HG00158, NA18611, HG00281, HG00139, HG00277, NA19720, HG00335, HG00106, HG01170, HG00236, HG00325, HG01072, HG01440, HG00427, HG00338, HG00159, NA18557, HG01048, HG01133, HG00326, HG00419, HG00253, NA20753, HG00108, HG00260, HG01353, HG00543, HG00313, HG00137, HG01183, HG00154, NA18544, HG00443, HG00268, HG00183, HG01187, HG01171, HG00282, HG00328, HG00653, HG00657, HG00475, HG00556, HG00320, HG00533, HG00583, NA18637, HG00500, HG00263, HG00275, NA18534, HG00708, HG00692, HG00635, NA18548, HG00740, HG01390, HG01047, HG00284, HG01073, HG00250, HG00690, HG00684, HG01101, HG00613, HG00525, NA19257, HG00463, HG00246, NA18570, HG01107, HG01148, HG00258, NA19390, NA18559, HG00625, HG00580, HG00375, NA19435, HG00638, HG00278, HG01174, HG01375, HG00607, NA19428, HG01137, HG00319, HG00256, NA12763, HG00662, HG00339, HG00125, HG00672, HG00312, HG00259, HG00421, HG00329, NA18636, NA18609, HG00186, HG00112, HG00274, HG01378, HG01125, HG00345, NA18549, HG01437, HG00581
Known GenesNEO1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672004
Frequency
Sample Size1151
Observed Gain0
Observed Loss152
Observed Complex0
Frequencyn/a


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