A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv694e201



Internal ID22760052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10751946..10754864hg38UCSC Ensembl
chr21:10757593..10760511hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg382919
hg192919
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2723130, esv2723127, esv2723125, esv2723132
SamplesSSM100, SSM071, SSM027, SSM024, SSM075, SSM079, SSM065, SSM087, SSM039, SSM073, SSM074, SSM042, SSM002, SSM028, SSM084, SSM021, SSM047, SSM029, SSM026, SSM089, SSM017, SSM019, SSM003, SSM031, SSM067, SSM044, SSM086, SSM033, SSM066, SSM085, SSM068, SSM040, SSM072, SSM082, SSM020, SSM015, SSM078, SSM016, SSM077, SSM022, SSM010, SSM091, SSM055, SSM070, SSM095, SSM025, SSM099, SSM043, SSM098, SSM012
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)dgv694e201
Frequency
Sample Size96
Observed Gain0
Observed Loss50
Observed Complex0
Frequencyn/a


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