A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv852e199



Internal ID22758625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15272568..15272716hg38UCSC Ensembl
chr3:15314075..15314223hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2660869, esv2671040
SamplesNA19394, NA18502, NA19701, HG01173, HG01356, NA19397, HG00608, NA19466, HG00671, HG00524, NA19399, HG01052, NA19704, NA11933, NA18917, NA19350, NA19359, NA19092, NA18545, NA19819, NA19057, NA18504, NA19377, NA18606, HG01518, HG00654, NA19443, NA19190, NA18526, NA19920, NA18510, NA19374, NA18563, NA19396, NA19381, NA19373, HG01350, NA19379, NA18519, NA19382, HG01351, HG00702, NA18923, NA20756, NA19198, NA12891, NA19916, NA18916, NA18582, NA19313, HG01083, NA19138, NA19384, NA19130, NA20541, NA19404, HG01134, HG01069, HG01067, NA20278, NA19383, HG00683, NA18874, HG00236, NA18977, NA19917, NA19238, NA19385, NA19317, NA19087, HG00427, NA19189, NA18520, NA19239, HG01048, NA20342, NA19921, NA19451, NA18638, HG01124, HG00313, HG00137, HG01136, HG00282, HG00596, NA19403, HG00557, NA19077, NA12003, NA19462, NA18933, HG00732, HG00653, HG00701, HG00657, NA19391, NA19236, HG00556, HG00275, NA18910, NA18566, HG01102, HG00324, HG01073, NA18573, NA19114, HG01197, HG00684, NA18856, NA19453, NA12892, NA18532, HG00613, NA18853, HG01334, NA18555, NA18570, NA18858, NA18593, NA20296, NA19401, NA19375, NA18632, HG00476, NA19440, NA19390, NA19834, NA19147, NA18559, NA19712, NA18628, NA19435, NA19331, NA19240, HG00278, NA19380, HG01174, HG01375, NA19334, NA19428, NA19324, NA19467, NA20516, NA19360, HG00418, HG00620, NA19376, NA19398, NA19328, HG00707, HG00111, NA20348, NA19472, HG00421, HG00656, NA19713, HG01254, NA19093, NA18636, NA18609, NA18873, NA19116, NA19711, NA19213, NA18552, NA19900, HG00252, NA18505, NA18488, HG01082, NA19312, HG01125, NA20322, NA19463, NA18511, NA18612, NA19429, NA19346, NA19074, NA18965
Known GenesSH3BP5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv852e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss180
Observed Complex0
Frequencyn/a


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