A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv817777



Internal ID16111733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98143221..98144052hg38UCSC Ensembl
Innerchr13:98795475..98796306hg19UCSC Ensembl
Innerchr13:97593476..97594307hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg38832
hg19832
hg18832
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv562866
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)nssv817777
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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