A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360



Internal ID15837638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67159114..67161508hg38UCSC Ensembl
Outerchr9:67158706..67162013hg38UCSC Ensembl
Innerchr9:40531333..40533727hg19UCSC Ensembl
Outerchr9:40530828..40534135hg19UCSC Ensembl
Innerchr9:40521333..40523727hg18UCSC Ensembl
Outerchr9:40520828..40524135hg18UCSC Ensembl
Innerchr9:40260616..40263010hg17UCSC Ensembl
Outerchr9:40260111..40263418hg17UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg383308
hg193308
hg183308
hg173308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8456
Supporting Variants
SamplesNA18853
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)nssv17360
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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