A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2744637



Internal ID10325607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:66496326..66496635hg38UCSC Ensembl
Outerchr11:66263797..66264106hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6970329, essv6834043, essv6940211, essv6737510
SamplesSSM007, SSM022, SSM010, SSM004
Known GenesDPP3
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)esv2744637
Frequency
Sample Size96
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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