A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562827



Internal ID16350236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97875185..97888965hg38UCSC Ensembl
Innerchr13:98527439..98541219hg19UCSC Ensembl
Innerchr13:97325440..97339220hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3813781
hg1913781
hg1813781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149451
SamplesHGDP00882
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562827
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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