A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015591



Internal ID22077222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:132640556..132848279hg38UCSC Ensembl
Outerchr4:132639974..132848778hg38UCSC Ensembl
Innerchr4:133561711..133769434hg19UCSC Ensembl
Outerchr4:133561129..133769933hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38208805
hg19208805
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156225
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015591
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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