A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545182



Internal ID18746258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:98266473..98266797hg38UCSC Ensembl
Outerchr9:98266425..98266847hg38UCSC Ensembl
Innerchr9:101028755..101029079hg19UCSC Ensembl
Outerchr9:101028707..101029129hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743929
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545182
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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