A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562228



Internal ID16349637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70159712..70198524hg38UCSC Ensembl
Innerchr13:70733844..70772656hg19UCSC Ensembl
Innerchr13:69631845..69670657hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3838813
hg1938813
hg1838813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3237n54
Supporting Variantsnssv813743, nssv813744
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562228
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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