A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562368



Internal ID16349777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:76549398..76612570hg38UCSC Ensembl
Innerchr13:77123533..77186705hg19UCSC Ensembl
Innerchr13:76021534..76084706hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3863173
hg1963173
hg1863173
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176359
SamplesHGDP01398
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562368
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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