A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv381e214



Internal ID22756275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20886539..20953797hg38UCSC Ensembl
chr14:21354698..21421956hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3867259
hg1967259
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3633700, esv3633694
SamplesHG03690, HG02890, HG02944, HG03378, HG02583, HG02272, NA19466, HG03548, HG03163, HG03175, NA18881, HG02419, NA18917, NA18486, HG02323, NA18530, HG03297, HG03139, HG02734, HG03577, HG03372, HG03069, NA18510, NA19374, HG03133, HG02621, NA18489, HG03452, HG02952, HG02383, NA20756, HG03370, HG03040, HG01242, HG02281, NA19923, HG02703, NA20278, NA18874, HG01628, NA19917, NA19137, HG03212, NA19172, HG02588, NA19036, HG03744, HG03380, HG02427, NA19239, NA19456, NA19025, HG03055, NA20127, NA20318, HG03270, HG02479, HG02570, NA19247, NA18934, HG02334, HG02582, NA18933, NA19984, HG03291, NA19455, NA19043, HG01088, HG00533, HG02307, HG02976, NA18907, HG03311, HG03123, HG01392, HG03472, HG02429, HG03136, HG00404, HG03446, HG02884, HG02283, NA19099, HG03391, NA19318, NA19395, HG02675, HG01990, HG02484, HG01896, HG02722, HG03567, NA18608, NA19401, NA19440, HG02667, NA19108, NA19019, HG02308, NA19473, HG02721, HG01958, NA19144, HG02314, NA19835, HG02179, HG02971, HG03442, NA19468, HG03063, HG03410, NA19116, NA19711, HG02681, HG02851, HG02284, HG03198, HG02808, NA19429, NA19431, HG03271
Known GenesECRP, RNASE3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv381e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss121
Observed Complex0
Frequencyn/a


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