A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561854



Internal ID16349263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:58498005..58545963hg38UCSC Ensembl
Innerchr13:59072139..59120097hg19UCSC Ensembl
Innerchr13:57970140..58018098hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg3847959
hg1947959
hg1847959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv812325
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561854
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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