A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562203



Internal ID16349612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:69084844..69127160hg38UCSC Ensembl
Innerchr13:69658976..69701292hg19UCSC Ensembl
Innerchr13:68556977..68599293hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3842317
hg1942317
hg1842317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175985
Samples1782681080_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562203
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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