A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154956



Internal ID22085461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88278786..88335053hg38UCSC Ensembl
Outerchr13:88276731..88338938hg38UCSC Ensembl
Innerchr13:88931041..88987308hg19UCSC Ensembl
Outerchr13:88928986..88991193hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3862208
hg1962208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008276
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154956
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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