A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3545546



Internal ID18746622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:131847944..131847967hg38UCSC Ensembl
Outerchr9:131847925..131847985hg38UCSC Ensembl
Innerchr9:134723331..134723354hg19UCSC Ensembl
Outerchr9:134723312..134723372hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9744293
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3545546
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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