A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv357e201



Internal ID22759715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46387637..46390596hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg192960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2714352, esv2714355
SamplesSSM100, SSM036, SSM083, SSM071, SSM027, SSM024, SSM045, SSM046, SSM011, SSM064, SSM079, SSM065, SSM087, SSM038, SSM097, SSM039, SSM093, SSM042, SSM041, SSM023, SSM028, SSM084, SSM021, SSM047, SSM069, SSM096, SSM026, SSM089, SSM017, SSM019, SSM035, SSM094, SSM032, SSM031, SSM067, SSM044, SSM014, SSM086, SSM033, SSM066, SSM068, SSM040, SSM072, SSM082, SSM020, SSM015, SSM016, SSM005, SSM080, SSM037, SSM077, SSM076, SSM022, SSM070, SSM095, SSM025, SSM034, SSM043, SSM098
Known Genes
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)dgv357e201
Frequency
Sample Size96
Observed Gain0
Observed Loss59
Observed Complex0
Frequencyn/a


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