A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv96e201



Internal ID20124983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:35150630..35151182hg38UCSC Ensembl
chr10:35439558..35440110hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2735350, esv2735339
SamplesSSM065, SSM013, SSM086, SSM033, SSM084, SSM099, SSM042, SSM039, SSM067, SSM041, SSM017, SSM069, SSM021, SSM023, SSM068, SSM004, SSM070, SSM080
Known GenesCREM
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)dgv96e201
Frequency
Sample Size96
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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