A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562223



Internal ID16349632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:70144506..70189465hg38UCSC Ensembl
Innerchr13:70718638..70763597hg19UCSC Ensembl
Innerchr13:69616639..69661598hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3844960
hg1944960
hg1844960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv813736, nssv813735
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562223
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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