A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6891102



Internal ID10285473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:7407380..7407724hg38UCSC Ensembl
Outerchr11:7428611..7428955hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744079
Supporting Variants
SamplesSSM097
Known GenesSYT9
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)essv6891102
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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