A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv335e201



Internal ID22759693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:32359969..32360642hg38UCSC Ensembl
chr16:32371290..32371963hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38674
hg19674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2714205, esv2714203
SamplesSSM036, SSM071, SSM027, SSM024, SSM064, SSM065, SSM087, SSM038, SSM039, SSM013, SSM009, SSM073, SSM093, SSM074, SSM002, SSM041, SSM092, SSM021, SSM047, SSM096, SSM026, SSM019, SSM032, SSM003, SSM044, SSM001, SSM085, SSM068, SSM040, SSM082, SSM020, SSM007, SSM015, SSM078, SSM016, SSM005, SSM037, SSM077, SSM022, SSM010, SSM091, SSM070, SSM095, SSM004, SSM099, SSM052, 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)dgv335e201
Frequency
Sample Size96
Observed Gain0
Observed Loss48
Observed Complex0
Frequencyn/a


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