A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545036



Internal ID18746112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:85403535..85404809hg38UCSC Ensembl
Outerchr9:85403490..85404905hg38UCSC Ensembl
Innerchr9:88018450..88019724hg19UCSC Ensembl
Outerchr9:88018405..88019820hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381416
hg191416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743783
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545036
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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