A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156249



Internal ID22086754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:157805876..157808406hg38UCSC Ensembl
Outerchr4:157801906..157808420hg38UCSC Ensembl
Innerchr4:158727028..158729558hg19UCSC Ensembl
Outerchr4:158723058..158729572hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg386515
hg196515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015725
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156249
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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