A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562867



Internal ID16350276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98226554..98262439hg38UCSC Ensembl
Innerchr13:98878808..98914693hg19UCSC Ensembl
Innerchr13:97676809..97712694hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3835886
hg1935886
hg1835886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149453
Samples1780862093_A
Known GenesFARP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562867
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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