A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661400



Internal ID9927505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23972427..23992229hg38UCSC Ensembl
Outerchr22:23972056..23992599hg38UCSC Ensembl
Innerchr22:24314616..24334422hg19UCSC Ensembl
Outerchr22:24314245..24334792hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3820544
hg1920548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv826e199
Supporting Variantsessv5998489, essv5678943, essv5401814, essv5780752, essv5661319, essv5508031, essv5535080, essv5531470, essv5959029, essv5563608, essv5785523, essv5663205, essv5660876, essv5456496, essv5467233, essv6187464, essv6019550, essv5702900, essv5396447, essv6209036, essv5459166, essv6076443, essv5639829, essv6590179, essv6530649, essv6535351, essv5635059, essv5466620, essv6587894, essv6420846, essv6401288, essv6022923, essv6343169, essv6289542, essv6031081, essv6384179, essv5463069, essv5777177, essv6158995, essv6292484, essv5708170, essv6436976, essv6267817, essv5718434, essv5889174, essv5398913, essv6263207, essv6471130, essv5954807, essv6212942, essv6591003, essv5513736, essv5570333, essv5852239, essv5833987, essv5994791, essv6090303, essv6196624, essv5899346, essv6567386, essv6315946, essv5666544, essv5991334, essv5486907, essv5868792, essv5612338, essv5441580, essv6348108, essv6152837, essv5795055, essv5816424, essv5962948, essv5872402, essv6461177, essv6455324, essv5893747, essv5864713, essv5553679, essv5579800, essv5403218, essv5576181, essv6255977, essv5827922, essv5676825, essv6542978, essv6484300, essv6163742, essv5616636, essv6185106, essv5455779, essv5456992, essv5465391, essv6404976, essv5976067, essv6054135, essv6527407, essv6421008, essv6070829, essv5526143, essv5744128, essv5561256, essv5782849, essv5714763
SamplesHG00114, HG00143, HG00231, HG00249, HG00361, HG00242, HG00100, HG00257, HG00151, HG00233, HG00318, HG00244, HG00181, HG00103, HG00177, HG00261, HG00337, HG00327, HG00127, HG00272, HG00122, HG00173, HG00330, HG00346, HG00247, HG00369, HG00270, HG00334, HG00185, HG00243, HG00158, HG00281, HG00139, HG00277, HG00335, HG00106, HG00236, HG00156, HG00325, HG00232, HG00309, HG00118, HG00338, HG00159, HG00326, HG00323, HG00253, HG00108, HG00260, HG00137, HG00188, HG00268, HG00266, HG00183, HG00176, HG00328, HG00368, HG00320, HG00344, HG00263, HG00275, HG00239, HG00324, HG00284, HG00273, HG00250, HG00373, HG00331, HG00117, HG00321, HG00140, HG01334, HG00152, HG00246, HG00126, HG00258, HG00124, HG00254, HG00119, HG00336, HG00285, HG00366, HG00375, HG00237, HG00319, HG00256, HG00339, HG00269, HG00125, HG00111, HG00329, HG00267, HG00174, HG00123, HG00112, HG00280, HG00343, HG00377, HG00372, HG00274, HG00252, HG00171, HG00180
Known GenesDDT, DDTL, GSTT2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661400
Frequency
Sample Size1151
Observed Gain0
Observed Loss103
Observed Complex0
Frequencyn/a


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