A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562862



Internal ID16350271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98142835..98144218hg38UCSC Ensembl
Innerchr13:98795089..98796472hg19UCSC Ensembl
Innerchr13:97593090..97594473hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381384
hg191384
hg181384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3343n54
Supporting Variantsnssv817772
Samples
Known GenesFARP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562862
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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