A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6763305



Internal ID9822909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:48923100..48923706hg38UCSC Ensembl
Outerchr11:48944652..48945258hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38607
hg19607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744485, esv2744493, esv2744495
Supporting Variants
SamplesSSM062
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)essv6763305
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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