A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154944



Internal ID22085449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:81114226..81135511hg38UCSC Ensembl
Outerchr13:81111157..81137787hg38UCSC Ensembl
Innerchr13:81688361..81709646hg19UCSC Ensembl
Outerchr13:81685292..81711922hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3826631
hg1926631
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008264
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154944
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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