A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665453



Internal ID9931558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6730005..6731811hg38UCSC Ensembl
Outerchr19:6729634..6732181hg38UCSC Ensembl
Innerchr19:6730016..6731822hg19UCSC Ensembl
Outerchr19:6729645..6732192hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6298024, essv6282278, essv6592389, essv5968580, essv6485660, essv5651366, essv5564007, essv5783023, essv5955950, essv6585168, essv5501049, essv5600149, essv6401406, essv6299754, essv6437522, essv6405843, essv5826637, essv6201831, essv6357344, essv5890125, essv5796956, essv5845353, essv5574149, essv6084621, essv6458755, essv5464046, essv5727860, essv6165372, essv6077536, essv5889642, essv6309940, essv6200406, essv6342362, essv5700849, essv5563879, essv5799324, essv6308951, essv5945506, essv6312251, essv5747817, essv5439626, essv5603839, essv5717774, essv6156600, essv5531902, essv6114774, essv6558372, essv5966937, essv5570323, essv6130909, essv6264160, essv5999106, essv5416324, essv5568051, essv6228235, essv5613178
SamplesHG00114, HG00143, HG00231, HG00249, HG00257, HG00244, HG00150, HG00261, HG00138, HG00251, HG00122, HG00247, HG00243, HG00158, HG00139, HG00120, HG00148, HG00106, HG00236, HG00156, HG00262, HG00232, HG00160, HG00118, HG00253, HG00264, HG00108, HG00260, HG00137, HG00133, HG00154, HG00245, HG00263, HG00239, HG00250, HG00157, HG00140, HG01334, HG00152, HG00146, HG00141, HG00258, HG00124, HG00254, HG00119, HG00136, HG00237, HG00116, HG00256, HG00125, HG00111, HG00259, HG00123, HG00112, HG00131, HG00252
Known GenesGPR108
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665453
Frequency
Sample Size1151
Observed Gain0
Observed Loss56
Observed Complex0
Frequencyn/a


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