A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv19962



Internal ID15832605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:67143720..67216978hg38UCSC Ensembl
Innerchr9:40475863..40549121hg19UCSC Ensembl
Innerchr9:40465863..40539121hg18UCSC Ensembl
Innerchr9:40205146..40278404hg17UCSC Ensembl
Outerchr9:40146338..40279322hg17UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3873259
hg1973259
hg1873259
hg17132985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv8456
Supporting Variants
SamplesNA18502
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)nssv19962
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer