A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545319



Internal ID18399709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111571023..111571599hg38UCSC Ensembl
Outerchr9:111570958..111571704hg38UCSC Ensembl
Innerchr9:114333303..114333879hg19UCSC Ensembl
Outerchr9:114333238..114333984hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744066
Samples
Known GenesPTGR1, ZNF483
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545319
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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