A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562560



Internal ID16349969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:84240779..84304501hg38UCSC Ensembl
Innerchr13:84814914..84878636hg19UCSC Ensembl
Innerchr13:83712915..83776637hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3863723
hg1963723
hg1863723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv816610
Samples
Known GenesLINC00333, MIR548F1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562560
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer