A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561865



Internal ID16002588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:60419209..60564352hg38UCSC Ensembl
Innerchr13:60993343..61138486hg19UCSC Ensembl
Innerchr13:59891344..60036487hg18UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg38145144
hg19145144
hg18145144
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3184n54
Supporting Variantsnssv812338
Samples
Known GenesTDRD3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561865
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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