A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544575



Internal ID18745651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14288048..14291410hg38UCSC Ensembl
Outerchr9:14287226..14291651hg38UCSC Ensembl
Innerchr9:14288047..14291409hg19UCSC Ensembl
Outerchr9:14287225..14291650hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg384426
hg194426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743322
Samples
Known GenesNFIB
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544575
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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