A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1418654



Internal ID15582438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:31283001..31298416hg38UCSC Ensembl
Innerchr10:31571930..31587345hg19UCSC Ensembl
Innerchr10:31611936..31627351hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3815416
hg1915416
hg1815416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv819388
Supporting Variants
SamplesAK1
Known Genes
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)nssv1418654
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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