A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1419201



Internal ID15582985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:78399287..78400504hg38UCSC Ensembl
Innerchr17:76395368..76396585hg19UCSC Ensembl
Innerchr17:73906963..73908180hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg381218
hg191218
hg181218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv820049
Supporting Variants
SamplesAK1
Known GenesPGS1
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)nssv1419201
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