A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9968



Internal ID15847880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:66157085..66166279hg38UCSC Ensembl
Outerchr2:66384217..66393411hg19UCSC Ensembl
Outerchr2:66237721..66246915hg18UCSC Ensembl
Outerchr2:66295868..66305062hg17UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg389195
hg199195
hg189195
hg179195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28257
SamplesNA19132
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)nsv9968
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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