A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1111e199



Internal ID11593370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:32658868..32668015hg38UCSC Ensembl
chr6:32626645..32635792hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg389148
hg199148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672407, esv2659336
SamplesHG00157, HG00152, HG00252, HG00318, HG00100, HG00127, HG00328, HG00171, HG00112, HG00274, HG00186, HG00245, HG00131, HG00155, HG00160, HG00261, HG00117, HG00189, HG00375, HG00368, HG00173, HG00326, HG00270, HG00139, HG00190, HG00122, HG00106, HG00111, HG00334, HG00280, HG00366, HG00177, HG00331, HG00146, HG00156, HG00188, HG00247, HG00342, HG00244, HG00266, HG00115, HG00321, HG00339, HG00158, HG00242, HG00250, HG00180, HG00259, HG00096, HG00141, HG00315, HG00330, HG00150, HG00178, HG00125, HG00258, HG00264, HG00174, HG00243, HG00276, HG00284, HG00357, HG00306, HG00267, HG00108, HG00233, HG00325, HG00260, HG00239, HG00265, HG00273, HG00151, HG00262, HG00123, HG00285, HG00142, HG00367, HG00251, HG00320, HG00324, HG00183, HG00143, HG00345, HG00278, HG00136, HG00126, HG00312, HG00327
Known GenesHLA-DQB1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1111e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss88
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer