A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562230



Internal ID16349639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70159712..70221718hg38UCSC Ensembl
Innerchr13:70733844..70795850hg19UCSC Ensembl
Innerchr13:69631845..69693851hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3862007
hg1962007
hg1862007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813746
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562230
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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