A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv9457



Internal ID15847369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:74326758..74431248hg38UCSC Ensembl
Outerchr16:74360656..74465146hg19UCSC Ensembl
Outerchr16:72918157..73022647hg18UCSC Ensembl
Outerchr16:72918157..73022647hg17UCSC Ensembl
Cytoband16q22.3
Allele length
AssemblyAllele length
hg38104491
hg19104491
hg18104491
hg17104491
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv23606, nssv26541, nssv26483, nssv24352, nssv26527, nssv26747, nssv21892, nssv24489, nssv23440, nssv24671, nssv23958, nssv24645, nssv25113, nssv21862
SamplesNA18502, NA11830, NA12155, NA18942, NA19132, NA18564, NA19144, NA12740, NA19173, NA18972, NA18552
Known GenesCLEC18B, LOC283922
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)nsv9457
Frequency
Sample Size31
Observed Gain1
Observed Loss10
Observed Complex0
Frequencyn/a


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