A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007977



Internal ID6720087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77269552..77276494hg38UCSC Ensembl
Innerchr17:75265634..75272576hg19UCSC Ensembl
Innerchr17:72777229..72784171hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg386943
hg196943
hg186943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3586545
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007977
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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