A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv85e201



Internal ID20124972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:3114923..3115921hg38UCSC Ensembl
chr10:3157115..3158113hg19UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38999
hg19999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2731184, esv2731228, esv2731206
SamplesSSM036, SSM008, SSM083, SSM024, SSM075, SSM045, SSM046, SSM064, SSM065, SSM087, SSM039, SSM013, SSM009, SSM073, SSM050, SSM074, SSM042, SSM002, SSM023, SSM028, SSM092, SSM084, SSM090, SSM021, SSM069, SSM029, SSM096, SSM089, SSM019, SSM032, SSM031, SSM067, SSM044, SSM001, SSM033, SSM085, SSM068, SSM040, SSM082, SSM020, SSM007, SSM015, SSM016, SSM005, SSM080, SSM037, SSM022, SSM091, SSM055, SSM070, SSM095, SSM025, SSM004, SSM043, SSM052, SSM049, SSM056, SSM012
Known GenesPFKP
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)dgv85e201
Frequency
Sample Size96
Observed Gain0
Observed Loss58
Observed Complex0
Frequencyn/a


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