A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562984



Internal ID16350393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103035231..103049023hg38UCSC Ensembl
Innerchr13:103687581..103701373hg19UCSC Ensembl
Innerchr13:102485582..102499374hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg3813793
hg1913793
hg1813793
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3369n54
Supporting Variantsnssv818825
Samples
Known GenesSLC10A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562984
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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