A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9414



Internal ID15847326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:28363140..28449790hg38UCSC Ensembl
Outerchr16:28374461..28461111hg19UCSC Ensembl
Outerchr16:28281962..28368612hg18UCSC Ensembl
Outerchr16:28281962..28368612hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3886651
hg1986651
hg1886651
hg1786651
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23902, nssv23295, nssv22917, nssv22928, nssv23814, nssv22044, nssv23278, nssv22134, nssv20260, nssv26135, nssv22473, nssv25057, nssv26761, nssv24139, nssv23875, nssv22784, nssv25271, nssv22074, nssv24174, nssv23267, nssv21902, nssv27862, nssv22056, nssv27869
SamplesNA11830, NA07029, NA18504, NA12155, NA18563, NA12802, NA18860, NA07048, NA10839, NA18975, NA19007, NA10863, NA19221, NA18537, NA18517, NA19240, NA19144, NA19173, NA18552
Known GenesEIF3C, EIF3CL, MIR6862-1, MIR6862-2
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)nsv9414
Frequency
Sample Size31
Observed Gain7
Observed Loss13
Observed Complex0
Frequencyn/a


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