A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154374



Internal ID22084879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:87128732..87145328hg38UCSC Ensembl
Outerchr8:87119551..87148212hg38UCSC Ensembl
Innerchr8:88140960..88157556hg19UCSC Ensembl
Outerchr8:88131779..88160440hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3828662
hg1928662
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004975
Samples
Known GenesCNBD1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154374
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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