A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664759



Internal ID9584178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:97841368..97849374hg38UCSC Ensembl
OuterchrX:97840897..97849794hg38UCSC Ensembl
InnerchrX:97096366..97104372hg19UCSC Ensembl
OuterchrX:97095895..97104792hg19UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg388898
hg198898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6268773, essv5656073, essv5974948, essv6224490, essv6090876, essv5694699, essv6576610, essv6446874, essv6446257, essv6392933, essv6245520, essv5653069, essv5438793, essv5986301, essv6122934, essv6561898, essv5931629, essv5804288, essv6455875, essv6172400, essv5876014, essv5401286, essv6450821, essv6292307, essv5577035, essv6541313, essv5534459, essv5629794, essv6560983, essv5769582, essv6558170, essv6431455, essv5919132, essv5754796, essv6067395, essv6157983, essv5743722, essv6163187, essv6032686, essv6140022, essv5635803, essv5624807, essv6053416, essv5807723, essv5943830, essv5663462, essv6465899, essv5852923, essv5718887, essv6371533, essv5411316, essv5682590, essv5921471, essv6405488, essv5693237, essv5990665, essv5780908, essv5673038, essv5489060, essv6551242, essv6372375, essv6534309, essv6282797, essv6261496, essv5897447, essv5461822, essv6369808, essv5458737, essv5606600, essv5493290, essv6522825, essv5708451, essv5980415, essv5577601, essv6022134, essv6071036, essv5933800, essv6552462, essv6531276, essv6374021, essv5887715, essv6301977, essv6111444, essv5833867, essv6082227, essv5956437, essv5415916, essv6478499, essv5687749, essv5961094, essv5654515, essv5647385, essv6489018, essv5728371, essv5831966, essv5546098
SamplesHG00593, HG00626, HG00403, HG01060, HG00650, HG00542, HG00442, HG01173, HG00592, HG00536, HG00608, HG00671, HG00559, HG00524, HG01079, HG01188, HG01066, HG00640, HG00566, HG00737, HG01051, HG00641, HG00589, HG01167, HG00702, HG00689, HG00448, HG00634, HG00736, HG00610, HG00590, HG00512, HG01069, HG00683, HG01170, HG01072, HG01176, HG00427, HG00637, HG01048, HG00530, HG00560, HG00731, HG00629, HG01187, HG00596, HG00732, HG00653, HG00577, HG00701, HG00475, HG00436, HG00556, HG00533, HG00583, HG00500, HG00619, HG00692, HG00635, HG00740, HG01047, HG00651, HG00404, HG01197, HG01182, HG01101, HG00613, HG00704, HG00463, HG01107, HG01204, HG01075, HG00611, HG01190, HG00625, HG00565, HG00580, HG00734, HG00638, HG00607, HG00662, HG00418, HG00620, HG00707, HG00672, HG00614, HG00578, HG00478, HG00421, HG00656, HG00698, HG00472, HG01082, HG00628, HG01097, HG00553
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664759
Frequency
Sample Size1151
Observed Gain0
Observed Loss96
Observed Complex0
Frequencyn/a


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