A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9935



Internal ID15847847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:61475414..61478254hg38UCSC Ensembl
Outerchr2:61702549..61705389hg19UCSC Ensembl
Outerchr2:61556053..61558893hg18UCSC Ensembl
Outerchr2:61614200..61617040hg17UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg382841
hg192841
hg182841
hg172841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv28111
SamplesNA19240
Known GenesXPO1
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)nsv9935
Frequency
Sample Size31
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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