A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547346



Internal ID18401736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14326802..14327077hg38UCSC Ensembl
Outerchr11:14326738..14327133hg38UCSC Ensembl
Innerchr11:14348348..14348623hg19UCSC Ensembl
Outerchr11:14348284..14348679hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746093
Samples
Known GenesRRAS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547346
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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