A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17057



Internal ID15835895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:38775821..38962517hg38UCSC Ensembl
Outerchr9:38771899..38963135hg38UCSC Ensembl
Innerchr9:38775818..38962514hg19UCSC Ensembl
Outerchr9:38771896..38963132hg19UCSC Ensembl
Innerchr9:38765818..38952514hg18UCSC Ensembl
Outerchr9:38761896..38953132hg18UCSC Ensembl
Innerchr9:38765818..38952514hg17UCSC Ensembl
Outerchr9:38761896..38953132hg17UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38191237
hg19191237
hg18191237
hg17191237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8446
Supporting Variants
SamplesNA18563
Known Genes
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)nssv17057
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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