A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154946



Internal ID22085451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83349400..83353770hg38UCSC Ensembl
Outerchr13:83342840..83356261hg38UCSC Ensembl
Innerchr13:83923535..83927905hg19UCSC Ensembl
Outerchr13:83916975..83930396hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3813422
hg1913422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008266
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154946
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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