A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746920



Internal ID18721166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93844839..93845026hg38UCSC Ensembl
Outerchr11:93844794..93845078hg38UCSC Ensembl
Innerchr11:93578005..93578192hg19UCSC Ensembl
Outerchr11:93577960..93578244hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38285
hg19285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3548173
Supporting Variants
Samples
Known GenesVSTM5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746920
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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