A curated catalogue of human genomic structural variation

Variant Details

Variant: esv2661713

Internal ID9581132
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63731451..63731559hg38UCSC Ensembl
chr20:62362803..62362911hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6220638, essv5432509, essv5681300, essv5582631, essv6337739, essv6587106, essv5401488, essv5564374, essv6439402, essv6450146, essv5710114, essv6147179, essv6494599, essv5433746, essv6162445, essv6506652, essv6580087, essv5880667, essv6534773, essv5549869, essv6310526, essv5747619, essv6131468, essv6445032, essv5539467, essv5892161, essv5906632, essv5766244, essv6454902, essv5995404, essv5564102, essv6047149, essv5726668, essv6207227, essv5978416, essv5768874, essv5737374, essv6249571, essv6023396, essv6320990, essv6188527, essv6076184, essv6239745, essv6201748, essv5627150, essv6302511, essv6529183, essv6119894, essv6011138, essv6420168, essv6578903, essv6176016, essv5952468, essv5567264, essv5641904, essv6198534, essv5428505, essv6531040, essv5987390, essv6390100, essv5693947
SamplesHG00313, NA19445, HG00252, HG00619, NA18534, NA18530, HG00418, NA19437, NA18612, NA18550, NA19359, HG01082, NA18947, NA18546, HG00701, HG00319, HG00253, NA18557, HG01171, HG00479, NA18632, NA18624, HG00250, NA12004, NA18622, NA19443, NA18623, NA19471, NA18636, HG00419, HG01113, HG01136, HG00276, NA19457, NA18633, NA18572, NA19102, NA19731, NA18564, NA19332, NA18613, HG00513, HG01070, NA18582, HG00443, HG00650, NA19431, NA18602, NA18577, HG00281, HG00422, HG00693, NA18611, HG00320, HG00275, HG00324, NA20528, NA18532, HG00442, HG00278, HG00531
Known GenesZGPAT
AnalysisNo reference, merging analysis
Pubmed ID23128226
Accession Number(s)esv2661713
Sample Size1151
Observed Gain0
Observed Loss61
Observed Complex0

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