A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10460



Internal ID15498737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:15755988..15816583hg38UCSC Ensembl
Outerchr4:15757611..15818206hg19UCSC Ensembl
Outerchr4:15366709..15427304hg18UCSC Ensembl
Outerchr4:15433880..15494475hg17UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3860596
hg1960596
hg1860596
hg1760596
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12569, nssv12942
SamplesNA19173, NA18502
Known GenesCD38
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)nsv10460
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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