A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv361e201



Internal ID22759719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:46405252..46413673hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg198422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2714377, esv2714375
SamplesSSM083, SSM071, SSM027, SSM024, SSM011, SSM079, SSM097, SSM039, SSM013, SSM093, SSM023, SSM090, SSM047, SSM069, SSM029, SSM096, SSM026, SSM019, SSM032, SSM003, SSM031, SSM067, SSM044, SSM014, SSM086, SSM033, SSM066, SSM068, SSM081, SSM040, SSM082, SSM020, SSM015, SSM016, SSM077, SSM022, SSM091, SSM070, SSM095, SSM025, SSM034, SSM004, 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)dgv361e201
Frequency
Sample Size96
Observed Gain0
Observed Loss44
Observed Complex0
Frequencyn/a


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