A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9574



Internal ID15500800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:59032062..59041378hg38UCSC Ensembl
Outerchr17:57109423..57118739hg19UCSC Ensembl
Outerchr17:54464205..54473521hg18UCSC Ensembl
Outerchr17:54464205..54473521hg17UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg389317
hg199317
hg189317
hg179317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23190
SamplesNA18942
Known GenesTRIM37
MethodOligo aCGH
AnalysisStatistical threshold = 5.0, minimum +/- log2 ratio = 0.25 and minimum number of probes = 2
PlatformAgilent-015686 Custom Human 244K CGH Microarray
Comments
ReferencePerry_et_al_2008
Pubmed ID18304495
Accession Number(s)nsv9574
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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