A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2666359

Internal ID9585778
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:323256..323301hg38UCSC Ensembl
Outerchr19:323099..323454hg38UCSC Ensembl
Innerchr19:323256..323301hg19UCSC Ensembl
Outerchr19:323099..323454hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6053440, essv6029947, essv6073196, essv6356713, essv5740691, essv5774414, essv6303628, essv6341811, essv6061830, essv5692688, essv5896691, essv6360432, essv5766592, essv5792477, essv6070263, essv6309706, essv5844408, essv6276582, essv5411863, essv6485067, essv5428034, essv5501904, essv5508163, essv5658140, essv6047896, essv5751908, essv5850548, essv5724259, essv5966084, essv6038886, essv5684631, essv6531729, essv5923261, essv5597409, essv5883843, essv5551940, essv6262070, essv6255037, essv5501811, essv5632924, essv5494930, essv5619389, essv6350390, essv6188809, essv6086915, essv6407522, essv5510979, essv6579717, essv5498411, essv6367167, essv5679108, essv5413068, essv6535564, essv6253793, essv5500177, essv5751991, essv5507969, essv6551188, essv5604949, essv6534835, essv6247273, essv6551493, essv5727137, essv5763387, essv5420255, essv6061106, essv6222517, essv6571643, essv5969211, essv6369734, essv6407284, essv6321293, essv6295051, essv5478395, essv6509927, essv6076124, essv6328395, essv5577020, essv6582628, essv5563521
SamplesNA20281, NA19137, HG00309, NA18870, NA19625, HG00257, HG01052, HG00551, NA19404, HG00328, NA20516, HG01083, HG00274, HG00186, NA19223, HG01079, NA19319, NA20296, NA20775, HG01197, HG00189, HG01488, HG01491, NA20786, NA19782, HG00139, HG00739, NA19834, HG00334, NA19108, NA19467, NA19438, HG00154, NA19463, NA18934, HG01140, NA12004, HG00308, HG00337, NA11994, NA19675, NA20504, NA20530, NA19440, HG00338, NA11831, NA19658, HG00243, HG00276, HG00284, NA19457, HG00357, NA20341, NA20769, HG01437, HG00268, HG01066, NA20795, HG00282, HG01356, NA18504, HG00103, HG01383, NA20756, HG01095, NA20289, HG00311, NA19446, NA11830, HG00281, HG00285, NA19225, NA19399, HG00324, HG01374, HG01102, NA20524, NA20502, HG00278, HG00136
Known GenesMIER2
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2666359
Sample Size1151
Observed Gain0
Observed Loss80
Observed Complex0

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