A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562628



Internal ID16350037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87113858..87148323hg38UCSC Ensembl
Innerchr13:87766113..87800578hg19UCSC Ensembl
Innerchr13:86564114..86598579hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3834466
hg1934466
hg1834466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816738
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562628
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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