A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154385



Internal ID22084890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:116618444..116621018hg38UCSC Ensembl
Outerchr8:116612244..116623338hg38UCSC Ensembl
Innerchr8:117630683..117633257hg19UCSC Ensembl
Outerchr8:117624483..117635577hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3811095
hg1911095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005021, nssv4005022, nssv4005023
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154385
Frequency
Sample Size131
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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