A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv819560



Internal ID15237525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:25216276..25216845hg38UCSC Ensembl
Innerchr8:25073792..25074361hg19UCSC Ensembl
Innerchr8:25129709..25130278hg18UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38570
hg19570
hg18570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1418844
SamplesAK1
Known GenesDOCK5
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)nsv819560
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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