A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv270e201



Internal ID22759628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:96708482..96709791hg38UCSC Ensembl
chr14:97174819..97176128hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg381310
hg191310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2749066, esv2749064
SamplesSSM100, SSM036, SSM008, SSM083, SSM071, SSM027, SSM045, SSM046, SSM064, SSM079, SSM065, SSM087, SSM097, SSM013, SSM050, SSM042, SSM088, SSM023, SSM028, SSM090, SSM047, SSM069, SSM061, SSM029, SSM062, SSM089, SSM017, SSM019, SSM035, SSM032, SSM003, SSM031, SSM044, SSM086, SSM066, SSM072, SSM082, SSM020, SSM007, SSM078, SSM016, SSM053, SSM080, SSM077, SSM022, SSM070, SSM025, SSM043, SSM098, SSM056
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)dgv270e201
Frequency
Sample Size96
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer