A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562832



Internal ID16350241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97875612..97899405hg38UCSC Ensembl
Innerchr13:98527866..98551659hg19UCSC Ensembl
Innerchr13:97325867..97349660hg18UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3823794
hg1923794
hg1823794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv817671
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562832
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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