A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819576



Internal ID15584277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:90263904..90393775hg38UCSC Ensembl
Innerchr3:90313054..90442925hg19UCSC Ensembl
Innerchr3:90395744..90525615hg18UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg38129872
hg19129872
hg18129872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418840
SamplesAK1
Known Genes
MethodSNP array
AnalysisNormalized bead intensity data and genotype calls were obtained with Illumina BeadStudio 3.1 software. Copy number variants (CNVs) were detected on the basis of deflected log R ratios.
PlatformGPL6985
Comments
ReferenceKim_et_al_2009
Pubmed ID19587683
Accession Number(s)nsv819576
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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