A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666359



Internal ID9585778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:323256..323301hg38UCSC Ensembl
Outerchr19:323099..323454hg38UCSC Ensembl
Innerchr19:323256..323301hg19UCSC Ensembl
Outerchr19:323099..323454hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6582628, essv5604949, essv6070263, essv6309706, essv6076124, essv5684631, essv5428034, essv5619389, essv6038886, essv6053440, essv5420255, essv6255037, essv5501904, essv6188809, essv6303628, essv6061830, essv5563521, essv6061106, essv5510979, essv5792477, essv5508163, essv5724259, essv6571643, essv6086915, essv6551188, essv6535564, essv6341811, essv5679108, essv5478395, essv6073196, essv5966084, essv5501811, essv6262070, essv5692688, essv5494930, essv6222517, essv5597409, essv5844408, essv6253793, essv5507969, essv5500177, essv5923261, essv6407284, essv5551940, essv6367167, essv6328395, essv5896691, essv6295051, essv6360432, essv5766592, essv6534835, essv6369734, essv6247273, essv6509927, essv5969211, essv5411863, essv6579717, essv5740691, essv6276582, essv5727137, essv6551493, essv5577020, essv6531729, essv6350390, essv6321293, essv5751908, essv5413068, essv5632924, essv5883843, essv5763387, essv6485067, essv6029947, essv5850548, essv5658140, essv5751991, essv5498411, essv6407522, essv5774414, essv6047896, essv6356713
SamplesHG00189, NA11830, HG01356, NA19399, HG01052, HG01079, HG00257, HG01374, HG01066, HG00103, NA12004, NA18504, NA18870, HG01140, HG00337, NA19446, NA19319, HG01488, NA20756, NA20795, NA20769, NA19457, HG01083, HG00334, NA19782, HG00311, HG00243, NA19404, HG00281, HG00139, NA20775, NA19137, NA11994, HG00309, HG00338, HG00739, NA11831, HG00154, HG00268, HG00282, NA18934, NA20524, HG00328, HG01095, NA19658, HG00551, HG01102, HG00324, HG00284, HG01197, HG01383, HG00276, NA19225, NA19625, NA19675, NA20296, NA19440, HG00285, NA19834, NA19108, HG00357, HG00136, HG00278, NA20530, HG00308, NA20504, NA19467, NA20516, NA20281, NA20341, HG01491, NA19438, NA19223, NA20289, HG00186, NA20786, HG00274, NA20502, NA19463, HG01437
Known GenesMIER2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666359
Frequency
Sample Size1151
Observed Gain0
Observed Loss80
Observed Complex0
Frequencyn/a


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