A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154964



Internal ID22085469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:97874636..97879211hg38UCSC Ensembl
Outerchr13:97862422..97881576hg38UCSC Ensembl
Innerchr13:98526890..98531465hg19UCSC Ensembl
Outerchr13:98514676..98533830hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3819155
hg1919155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008293
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154964
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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