A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3544918



Internal ID18745994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73403147..73412123hg38UCSC Ensembl
Outerchr9:73402085..73413084hg38UCSC Ensembl
Innerchr9:76018063..76027039hg19UCSC Ensembl
Outerchr9:76017001..76028000hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3811000
hg1911000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9743665
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3544918
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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