A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563430



Internal ID16350839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113971527..114164720hg38UCSC Ensembl
Innerchr13:114740938..114930195hg19UCSC Ensembl
Innerchr13:113759040..113948297hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38193194
hg19189258
hg18189258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820870
Samples
Known GenesRASA3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563430
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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