A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562995



Internal ID16350404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:103905491..104280836hg38UCSC Ensembl
Innerchr13:104557841..104933186hg19UCSC Ensembl
Innerchr13:103355842..103731187hg18UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg38375346
hg19375346
hg18375346
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv818846
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562995
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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