A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154388



Internal ID22084893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:123157393..123270144hg38UCSC Ensembl
Outerchr8:123155027..123278634hg38UCSC Ensembl
Innerchr8:124169633..124282384hg19UCSC Ensembl
Outerchr8:124167267..124290874hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg38123608
hg19123608
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005045
Samples
Known GenesC8orf76, FAM83A, FAM83A-AS1, MIR4663, ZHX1, ZHX1-C8ORF76
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154388
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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