A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2758569



Internal ID9634028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:56712636..56861315hg38UCSC Ensembl
InnerchrX:56739069..56887748hg19UCSC Ensembl
InnerchrX:56755794..56904473hg18UCSC Ensembl
InnerchrX:56622090..56770769hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg38148680
hg19148680
hg18148680
hg17148680
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsesv2758867
Supporting Variantsessv2848, essv3199, essv20937, essv17949, essv23253, essv2323, essv4032, essv372, essv3987, essv24701, essv14356, essv3538, essv5366, essv3378, essv21823, essv9762, essv6898, essv23005, essv12544, essv16025, essv15819, essv1970, essv2617, essv24923, essv6394, essv2264, essv4869, essv5462, essv21704, essv12819, essv22633, essv22912, essv15408, essv13708, essv2225, essv17425, essv10091, essv11174, essv8606, essv9357, essv13538, essv3169, essv10271, essv9183, essv9157, essv22154, essv19219, essv1454, essv19696, essv13776, essv1365, essv18334, essv18934, essv23513, essv17349, essv8941, essv7797, essv11813, essv22032, essv7428, essv24283, essv20302, essv16744, essv9895, essv19601, essv13470, essv12490, essv4257, essv2672, essv4668, essv19750, essv12719, essv23532, essv3752
SamplesNA19203, NA11829, NA18561, NA19145, NA18603, NA07029, NA12801, NA12248, NA18959, NA10857, NA19098, NA12155, NA18967, NA18563, NA19192, NA18944, NA18940, NA12812, NA10835, NA19119, NA18635, NA18860, NA18558, NA18960, NA06993, NA19130, NA12005, NA18970, NA11994, NA19207, NA19128, NA18966, NA18990, NA19239, NA19200, NA19007, NA18605, NA12760, NA12752, NA19120, NA19194, NA12003, NA18572, NA11839, NA10838, NA18856, NA18853, NA12264, NA12144, NA19160, NA10856, NA18945, NA19012, NA18974, NA12043, NA18953, NA18914, NA18632, NA18961, NA18863, NA18501, NA06994, NA18971, NA19223, NA19211, NA18521, NA18506, NA18872, NA18623, NA12154, NA07034, NA18622, NA19153, NA18965
Known GenesLOC550643, UQCRBP1
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)esv2758569
Frequency
Sample Size270
Observed Gain60
Observed Loss14
Observed Complex0
Frequencyn/a


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