A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562386



Internal ID16349795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:77697718..77698388hg38UCSC Ensembl
Innerchr13:78271853..78272523hg19UCSC Ensembl
Innerchr13:77169854..77170524hg18UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38671
hg19671
hg18671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3262n54
Supporting Variantsnssv815812
Samples
Known GenesMIR3665, SLAIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562386
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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