A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819702



Internal ID15237667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:4679602..4680140hg38UCSC Ensembl
Innerchr9:4679602..4680140hg19UCSC Ensembl
Innerchr9:4669602..4670140hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38539
hg19539
hg18539
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418995
SamplesAK1
Known GenesCDC37L1
MethodOligo aCGH
AnalysisThe array was scanned with Agilent DNA microarray scanner at 2 micron resolution. The resulting image was extracted by Agilent's Feature Extraction software. The log2 ratios were analyzed using NEXUS software. Each aberration call was manually checked to confirm the accuracy of the calls.
PlatformGSE19651
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nsv819702
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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