A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv32e199



Internal ID20123334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25287554..25335401hg38UCSC Ensembl
chr1:25614045..25661892hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3847848
hg1947848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2677938, esv2657070
SamplesHG00323, HG00157, HG00313, HG00152, HG00252, HG00344, HG00100, HG00127, HG00171, HG00274, HG00131, HG00155, HG00310, HG00261, HG00189, HG00375, HG00368, HG00173, HG00148, HG00122, HG00334, HG00335, HG00366, HG00177, HG00146, HG00319, HG00253, HG00156, HG00188, HG00353, HG00342, HG00266, HG00321, HG00339, HG00158, HG00179, HG00337, HG00140, HG00096, HG00231, HG00315, HG00338, HG00150, HG00258, HG00174, HG00243, HG00254, HG00343, HG00133, HG00124, HG00108, HG00268, HG00185, HG00263, HG00176, HG00239, HG00265, HG00273, HG00249, HG00116, HG00277, HG00329, HG00236, HG00181, HG01334, HG00138, HG00262, HG00118, HG00281, HG00285, HG00251, HG00119, HG00275, HG00324, HG00137, HG00143, HG00336, HG00272, HG00278, HG00136, HG00126, HG00327
Known GenesRHD
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv32e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss82
Observed Complex0
Frequencyn/a


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