A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156873



Internal ID22087274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18585234..18587607hg38UCSC Ensembl
Outerchr8:18580219..18588702hg38UCSC Ensembl
Innerchr8:18442744..18445117hg19UCSC Ensembl
Outerchr8:18437729..18446212hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg388484
hg198484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020964
Samples
Known GenesPSD3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156873
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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