A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746619



Internal ID18720865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:61340332..61340642hg38UCSC Ensembl
Outerchr11:61340282..61340718hg38UCSC Ensembl
Innerchr11:61107804..61108114hg19UCSC Ensembl
Outerchr11:61107754..61108190hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547872
Supporting Variants
Samples
Known GenesDAK
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746619
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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