A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154369



Internal ID22084874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:78266379..78273093hg38UCSC Ensembl
Outerchr8:78262264..78276379hg38UCSC Ensembl
Innerchr8:79178614..79185328hg19UCSC Ensembl
Outerchr8:79174499..79188614hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3814116
hg1914116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004962, nssv4004960, nssv4004963, nssv4004961
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154369
Frequency
Sample Size131
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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