A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156263



Internal ID22084739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:167766475..168010639hg38UCSC Ensembl
Outerchr4:167763212..168014450hg38UCSC Ensembl
Innerchr4:168687626..168931790hg19UCSC Ensembl
Outerchr4:168684363..168935601hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38251239
hg19251239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016964
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156263
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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