A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562849



Internal ID16003572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98142301..98143785hg38UCSC Ensembl
Innerchr13:98794555..98796039hg19UCSC Ensembl
Innerchr13:97592556..97594040hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381485
hg191485
hg181485
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3341n54
Supporting Variantsnssv817751
Samples
Known GenesFARP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562849
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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