A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746056



Internal ID18720302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10271269..10272261hg38UCSC Ensembl
Outerchr11:10271134..10272330hg38UCSC Ensembl
Innerchr11:10292816..10293808hg19UCSC Ensembl
Outerchr11:10292681..10293877hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547309
Supporting Variants
Samples
Known GenesSBF2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746056
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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