A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156213



Internal ID22086718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:108270936..108274897hg38UCSC Ensembl
Outerchr4:108269407..108278509hg38UCSC Ensembl
Innerchr4:109192092..109196053hg19UCSC Ensembl
Outerchr4:109190563..109199665hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg389103
hg199103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015430
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156213
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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