A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817779



Internal ID16111735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98413701..98429271hg38UCSC Ensembl
Innerchr13:99065955..99081525hg19UCSC Ensembl
Innerchr13:97863956..97879526hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3815571
hg1915571
hg1815571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562870
Supporting Variants
Samples
Known GenesFARP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv817779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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