A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv10442



Internal ID15498719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8619753..8639554hg38UCSC Ensembl
Outerchr4:8621480..8641280hg19UCSC Ensembl
Outerchr4:8672380..8692180hg18UCSC Ensembl
Outerchr4:8739551..8759351hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3819802
hg1919801
hg1819801
hg1719801
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv12024, nssv29162, nssv12591, nssv12078, nssv12189, nssv28837, nssv11750, nssv12732, nssv12034, nssv11737, nssv12091, nssv29048, nssv13613, nssv13800, nssv12359, nssv11626, nssv12938, nssv12123, nssv11747, nssv12807, nssv11522, nssv11755, nssv11758, nssv11496
SamplesNA12802, NA18975, NA19173, NA10839, NA10847, NA18972, NA19144, NA18860, NA07029, NA10863, NA12155, NA18563, NA12740, NA07048, NA18502, NA12872, NA18564, NA19221, NA18552, NA19132, NA11830, NA19240, NA18853, NA18980
Known GenesCPZ
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)nsv10442
Frequency
Sample Size31
Observed Gain24
Observed Loss0
Observed Complex0
Frequencyn/a


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