A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv478e215



Internal ID22785988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15813503..15822502hg38UCSC Ensembl
chr9:15813501..15822500hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3544594, esv3544593
Samples
Known GenesCCDC171
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)dgv478e215
Frequency
Sample Size767
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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