A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661713



Internal ID9581132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63731451..63731559hg38UCSC Ensembl
chr20:62362803..62362911hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5428505, essv6239745, essv6119894, essv5681300, essv5564102, essv6506652, essv5978416, essv6047149, essv6320990, essv6162445, essv6445032, essv5987390, essv5401488, essv6011138, essv6131468, essv6454902, essv5880667, essv5627150, essv5693947, essv6580087, essv5433746, essv6439402, essv6249571, essv5747619, essv6147179, essv5952468, essv6198534, essv6390100, essv6176016, essv6494599, essv6337739, essv5564374, essv6529183, essv6450146, essv5582631, essv5567264, essv5766244, essv6310526, essv6207227, essv5539467, essv5737374, essv5641904, essv5432509, essv6587106, essv6420168, essv5549869, essv6201748, essv6534773, essv5995404, essv6023396, essv6076184, essv6188527, essv6220638, essv5726668, essv6302511, essv5906632, essv6531040, essv5768874, essv5892161, essv6578903, essv5710114
SamplesHG00650, HG00442, NA18947, NA19332, NA19359, NA12004, NA18530, NA19443, NA18633, NA18602, HG00693, NA18550, HG01070, NA18582, NA19457, NA18611, HG00281, NA19731, HG00422, NA19471, NA18557, NA19445, HG00419, HG00253, HG00313, HG01136, NA18613, NA19437, HG00443, HG01171, HG00701, HG00320, HG00275, NA18572, NA18534, HG00619, HG00324, HG00250, HG00531, HG00479, NA18532, HG00276, NA18546, NA18632, NA18564, HG00278, HG01113, HG00319, HG00418, HG00513, NA18636, NA19102, NA20528, HG00252, HG01082, NA18624, NA18623, NA18612, NA18622, NA19431, NA18577
Known GenesZGPAT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661713
Frequency
Sample Size1151
Observed Gain0
Observed Loss61
Observed Complex0
Frequencyn/a


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