A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746460



Internal ID18374020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:47740412..47741686hg38UCSC Ensembl
Outerchr11:47740285..47741847hg38UCSC Ensembl
Innerchr11:47761964..47763238hg19UCSC Ensembl
Outerchr11:47761837..47763399hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg381563
hg191563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547713
Supporting Variants
Samples
Known GenesFNBP4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746460
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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