A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744083



Internal ID18371643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113105328..113106806hg38UCSC Ensembl
chr9:115867608..115869086hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381479
hg191479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545336
Supporting Variants
Samples
Known GenesFAM225B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744083
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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