A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892020



Internal ID18839730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61938021..61955173hg38UCSC Ensembl
Outerchr11:61938021..61955173hg38UCSC Ensembl
Innerchr11:61705493..61722645hg19UCSC Ensembl
Outerchr11:61705493..61722645hg19UCSC Ensembl
Innerchr11:61462069..61479221hg18UCSC Ensembl
Outerchr11:61462069..61479221hg18UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3817153
hg1917153
hg1817153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786916
Samples
Known GenesBEST1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892020
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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