A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154957



Internal ID22085462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:88821001..88946208hg38UCSC Ensembl
Outerchr13:88815813..88948595hg38UCSC Ensembl
Innerchr13:89473255..89598462hg19UCSC Ensembl
Outerchr13:89468067..89600849hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38132783
hg19132783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4008277
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154957
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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