A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562869



Internal ID16350278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98413701..98428843hg38UCSC Ensembl
Innerchr13:99065955..99081097hg19UCSC Ensembl
Innerchr13:97863956..97879098hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3815143
hg1915143
hg1815143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3345n54
Supporting Variantsnssv817778
Samples
Known GenesFARP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562869
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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