A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997111



Internal ID7081081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38764950..39062907hg38UCSC Ensembl
Innerchr9:38764947..39062904hg19UCSC Ensembl
Innerchr9:38754947..39052904hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38297958
hg19297958
hg18297958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586593
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997111
Frequency
Sample Size3
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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