A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9746421



Internal ID18373981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43888081..43888345hg38UCSC Ensembl
Outerchr11:43888014..43888393hg38UCSC Ensembl
Innerchr11:43909631..43909895hg19UCSC Ensembl
Outerchr11:43909564..43909943hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3547674
Supporting Variants
Samples
Known GenesALKBH3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9746421
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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