A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv287e201



Internal ID22759645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105652396..105771527hg38UCSC Ensembl
chr14:106118733..106237864hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38119132
hg19119132
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2743186, esv2741452, esv2742451, esv2742898, esv2740796, esv2741660, esv2742624, esv2741733, esv2743101, esv2742419, esv2741944, esv2740849, esv2742245, esv2741343, esv2741549, esv2741476, esv2742519, esv2741047, esv2742659, esv2741879, esv2742860, esv2742499, esv2742622, esv2742638, esv2743191, esv2741765, esv2742108, esv2741577, esv2742078, esv2742141, esv2741734, esv2743421, esv2741682, esv2742396, esv2743376, esv2743025, esv2742699, esv2740879, esv2742422, esv2741015, esv2742658, esv2742817, esv2741652, esv2742183, esv2742625, esv2740926, esv2741970, esv2742209, esv2742497, esv2742432, esv2742942, esv2742142, esv2741993, esv2741156, esv2740909, esv2742046, esv2742252, esv2741813, esv2741014, esv2742109, esv2742023, esv2742556, esv2742077, esv2741110, esv2742494, esv2741324, esv2741267, esv2741232, esv2741654, esv2743149, esv2742594, esv2741524, esv2741398, esv2743340, esv2742521, esv2742896, esv2740945, esv2743235, esv2741376, esv2742538, esv2743236, esv2741919, esv2743022, esv2742816, esv2742182, esv2742433, esv2742000, esv2741323, esv2742229, esv2741123
SamplesSSM100, SSM059, SSM036, SSM008, SSM083, SSM071, SSM024, SSM075, SSM045, SSM046, SSM011, SSM079, SSM065, SSM097, SSM039, SSM013, SSM009, SSM073, SSM093, SSM050, SSM074, SSM042, SSM088, SSM057, SSM023, SSM028, SSM092, SSM090, SSM021, SSM018, SSM069, SSM061, SSM029, SSM062, SSM026, SSM089, SSM017, SSM019, SSM035, SSM094, SSM031, SSM067, SSM001, SSM033, SSM006, SSM068, SSM081, SSM040, SSM072, SSM082, SSM078, SSM016, SSM053, SSM005, SSM080, SSM077, SSM076, SSM010, SSM095, SSM025, SSM034, SSM004, SSM099, SSM043, SSM098, SSM049, SSM056
Known GenesELK2AP
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)dgv287e201
Frequency
Sample Size96
Observed Gain0
Observed Loss67
Observed Complex0
Frequencyn/a


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