A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669669



Internal ID9935774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1977817..1980623hg38UCSC Ensembl
Outerchr19:1977446..1980993hg38UCSC Ensembl
Innerchr19:1977816..1980622hg19UCSC Ensembl
Outerchr19:1977445..1980992hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383548
hg193548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6431620, essv6453059, essv6288432, essv5604751, essv5462296, essv6484940, essv5481075, essv5420560, essv5623071, essv6295860, essv5399370, essv5977734, essv6320973, essv5768324, essv5931345, essv6418431, essv6007041, essv6170493, essv5924026, essv6477577, essv6373260, essv5791505, essv6055555, essv6167319, essv5781116, essv6483705, essv6526694, essv5889097, essv6551542, essv5563719, essv5413894, essv6596021, essv5967274, essv5822252, essv5772067, essv6516196, essv5894114, essv5679310, essv5646463, essv6432990, essv5528252, essv5873120, essv5802937, essv5407977, essv5666550, essv6411910, essv5668978, essv5593543, essv5971231, essv5982306, essv6090525, essv5776994, essv6390733, essv6087448, essv5811203, essv6238793, essv6420985, essv5823105, essv6076528, essv6440534, essv6276271, essv6355413, essv6244322, essv5717643, essv5522937, essv5415691, essv6429261, essv6348315, essv6264345, essv6194551, essv5513568, essv6380269, essv6446592, essv6416958, essv6287034, essv6209883, essv6345352, essv5617429, essv6188964, essv5498971, essv6585833, essv5590698, essv5836276, essv5663259, essv6223123, essv6118136, essv5657193, essv6516858, essv6563962, essv5938860, essv6011710, essv6311141, essv5603234, essv5716135, essv5646292, essv5523261, essv5883062, essv5785033, essv6085894, essv6268880, essv6324138, essv5834490, essv6419102, essv6010700, essv6014595, essv5760988, essv6492984, essv6128219, essv5782092, essv6416009, essv5962499, essv5411328, essv6585771, essv5731844, essv6064710, essv5916749, essv5528388, essv6538717, essv6397947, essv6366076, essv6035700, essv6514202, essv6148766, essv6336813, essv6368534, essv5734485, essv5615656, essv6257022, essv6092974, essv6150993, essv6488653, essv5626559, essv6451540, essv6131036, essv6194645, essv6193488, essv5691524, essv5537888, essv5564419, essv6154805, essv6474295, essv5558092, essv6331548, essv6145218, essv6007262, essv6275491, essv5511199, essv5902683, essv5457323, essv5587983, essv6435928, essv6195504, essv6463114, essv6594431, essv6078161, essv6190407, essv5746857, essv6298107, essv6187870, essv6312509, essv5736331, essv6531791, essv6081321, essv5647846, essv6488772, essv5874479, essv5931080, essv5787834, essv5598058, essv5456040, essv6440485, essv6533497, essv5709177, essv5891235, essv6234695, essv5608019, essv6337278, essv5720619, essv5561681, essv5715823, essv6469507, essv6595609, essv5566597, essv5499190, essv5695699, essv6289136, essv6509975, essv5890108, essv5898384, essv6185728, essv5672438, essv6248961, essv6057649, essv6536402, essv6166628, essv6446376, essv6019276, essv5434241, essv5674660, essv5990923, essv6258802, essv5950154, essv5516623, essv5485240, essv6226927, essv5990215, essv5851875, essv5781078, essv5967050, essv5698024
SamplesHG00626, HG00403, HG00114, HG00650, HG00542, HG00442, HG00592, HG00143, HG00536, HG00231, HG00608, HG00142, HG00249, HG00671, HG00524, HG00187, HG00100, HG00257, HG00315, HG00151, HG00367, HG00318, HG00244, HG00181, HG00699, HG00566, HG00179, HG00449, HG00177, HG00150, HG00654, HG00261, HG00693, HG00337, HG00327, HG00271, HG00663, HG00138, HG00589, HG00272, HG00251, HG00501, HG00122, HG00702, HG00689, HG00448, HG00330, HG00610, HG00346, HG00247, HG00334, HG00185, HG00537, HG00243, HG00590, HG00158, HG00512, HG00281, HG00139, HG00277, HG00120, HG00683, HG00335, HG00148, HG00106, HG00236, HG00156, HG00325, HG00262, HG00232, HG00534, HG00422, HG00705, HG00309, HG00182, HG00427, HG00160, HG00118, HG00338, HG00159, HG00326, HG00178, HG00323, HG00530, HG00419, HG00253, HG00464, HG00108, HG00260, HG00543, HG00313, HG00137, HG00133, HG00188, HG00154, HG00149, HG00443, HG00268, HG00266, HG00183, HG00176, HG00282, HG00596, HG00557, HG00328, HG00428, HG00653, HG00701, HG00657, HG00475, HG00436, HG00556, HG00320, HG00584, HG00533, HG00583, HG00344, HG00500, HG00263, HG00275, HG00619, HG00239, HG00708, HG00692, HG00635, HG00324, HG00284, HG00273, HG00651, HG00250, HG00690, HG00404, HG00373, HG00531, HG00479, HG00331, HG00684, HG00117, HG00613, HG00525, HG00321, HG00157, HG00140, HG01334, HG00276, HG00152, HG00146, HG00704, HG00463, HG00141, HG00246, HG00126, HG00258, HG00611, HG00476, HG00124, HG00155, HG00254, HG00119, HG00336, HG00285, HG00265, HG00625, HG00565, HG00353, HG00580, HG00375, HG00357, HG00136, HG00278, HG00473, HG00607, HG00237, HG00319, HG00116, HG00256, HG00662, HG00418, HG00620, HG00339, HG00269, HG00125, HG00707, HG00672, HG00614, HG00111, HG00513, HG00478, HG00259, HG00421, HG00329, HG00656, HG00342, HG00174, HG00123, HG00310, HG00186, HG00698, HG00280, HG00343, HG00274, HG00252, HG00595, HG00472, HG00628, HG00171, HG00345, HG00180, HG00437, HG00581
Known GenesCSNK1G2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669669
Frequency
Sample Size1151
Observed Gain0
Observed Loss210
Observed Complex0
Frequencyn/a


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