A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562850



Internal ID16003573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98142480..98143646hg38UCSC Ensembl
Innerchr13:98794734..98795900hg19UCSC Ensembl
Innerchr13:97592735..97593901hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381167
hg191167
hg181167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3341n54
Supporting Variantsnssv817752
Samples
Known GenesFARP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562850
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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