A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545338



Internal ID18746414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113174821..113175082hg38UCSC Ensembl
Outerchr9:113174780..113175124hg38UCSC Ensembl
Innerchr9:115937101..115937362hg19UCSC Ensembl
Outerchr9:115937060..115937404hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38345
hg19345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744085
Samples
Known GenesFKBP15
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545338
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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