A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562871



Internal ID16350280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98418758..98431952hg38UCSC Ensembl
Innerchr13:99071012..99084206hg19UCSC Ensembl
Innerchr13:97869013..97882207hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3813195
hg1913195
hg1813195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817780
Samples
Known GenesFARP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562871
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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