A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6672956



Internal ID10090499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:56500276..56512254hg38UCSC Ensembl
Outerchr11:56267752..56279730hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811979
hg1911979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744540
Supporting Variants
SamplesSSM031
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)essv6672956
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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