A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3547697



Internal ID18402087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:46014700..46014945hg38UCSC Ensembl
Outerchr11:46014607..46015060hg38UCSC Ensembl
Innerchr11:46036251..46036496hg19UCSC Ensembl
Outerchr11:46036158..46036611hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9746444
Samples
Known GenesPHF21A
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3547697
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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