A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2743928



Internal ID10324898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:1428522..1429849hg38UCSC Ensembl
Outerchr11:1449752..1451079hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg381328
hg191328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6912403, essv6768354, essv6907296, essv6743880, essv6965470, essv6976801, essv6709877, essv6856900, essv6737745, essv6735051, essv6833432, essv6749534, essv6958958, essv6876507, essv6842263, essv6695351, essv6970589, essv6770120, essv6915957
SamplesSSM008, SSM027, SSM064, SSM087, SSM050, SSM002, SSM028, SSM092, SSM084, SSM029, SSM026, SSM006, SSM015, SSM016, SSM053, SSM037, SSM010, SSM049, SSM056
Known GenesBRSK2
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)esv2743928
Frequency
Sample Size96
Observed Gain0
Observed Loss19
Observed Complex0
Frequencyn/a


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