A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv12911



Internal ID15832083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:291563..381200hg38UCSC Ensembl
Outerchr6:290368..381993hg38UCSC Ensembl
Innerchr6:291563..381200hg19UCSC Ensembl
Outerchr6:290368..381993hg19UCSC Ensembl
Innerchr6:236563..326200hg18UCSC Ensembl
Outerchr6:235368..326993hg18UCSC Ensembl
Innerchr6:236563..326200hg17UCSC Ensembl
Outerchr6:235368..326993hg17UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3891626
hg1991626
hg1891626
hg1791626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv10799
Supporting Variants
SamplesNA12872
Known GenesDUSP22
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)nssv12911
Frequency
Sample Size31
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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