A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154391



Internal ID22084896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:129104450..129115872hg38UCSC Ensembl
Outerchr8:129099922..129124380hg38UCSC Ensembl
Innerchr8:130116696..130128118hg19UCSC Ensembl
Outerchr8:130112168..130136626hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3824459
hg1924459
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005048, nssv4005050, nssv4005049
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154391
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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