A curated catalogue of human genomic structural variation




Variant Details

Variant: esv998319



Internal ID7081722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57696663..57698133hg38UCSC Ensembl
Innerchr17:55774024..55775494hg19UCSC Ensembl
Innerchr17:53129023..53130493hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381471
hg191471
hg181471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3587014
SamplesHuRef
Known Genes
MethodOligo aCGH
Analysis
PlatformNot Submitted
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv998319
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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