A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156212



Internal ID22086717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107590598..107593342hg38UCSC Ensembl
Outerchr4:107588998..107595118hg38UCSC Ensembl
Innerchr4:108511755..108514498hg19UCSC Ensembl
Outerchr4:108510155..108516274hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg386121
hg196120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015429
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156212
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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