A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154346



Internal ID22084851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:40326278..40331992hg38UCSC Ensembl
Outerchr8:40324598..40335391hg38UCSC Ensembl
Innerchr8:40183797..40189511hg19UCSC Ensembl
Outerchr8:40182117..40192910hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3810794
hg1910794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004848, nssv4004849, nssv4004463, nssv4004464, nssv4004850, nssv4004845, nssv4004847, nssv4004852, nssv4004853, nssv4004851, nssv4004846
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154346
Frequency
Sample Size131
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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