A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6845893



Internal ID10244786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:95030261..95056982hg38UCSC Ensembl
Outerchr11:94763425..94790146hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3826722
hg1926722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2744933
Supporting Variants
SamplesSSM085
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)essv6845893
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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