A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv8168



Internal ID15846080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:79174529..79225198hg38UCSC Ensembl
Outerchr7:78803845..78854514hg19UCSC Ensembl
Outerchr7:78641781..78692450hg18UCSC Ensembl
Outerchr7:78448496..78499165hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3850670
hg1950670
hg1850670
hg1750670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16349, nssv18207
SamplesNA19132, NA19173
Known GenesMAGI2
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)nsv8168
Frequency
Sample Size31
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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