A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154974



Internal ID22085479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111527258..111544020hg38UCSC Ensembl
Outerchr13:111524280..111551547hg38UCSC Ensembl
Innerchr13:112179605..112196367hg19UCSC Ensembl
Outerchr13:112176627..112203894hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3827268
hg1927268
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008312
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154974
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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