A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154929



Internal ID22085434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:68091318..68128636hg38UCSC Ensembl
Outerchr13:68090067..68130415hg38UCSC Ensembl
Innerchr13:68665450..68702768hg19UCSC Ensembl
Outerchr13:68664199..68704547hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3840349
hg1940349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008167
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154929
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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