A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156129



Internal ID22086634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:27077228..27375630hg38UCSC Ensembl
Outerchr4:27070110..27385573hg38UCSC Ensembl
Innerchr4:27078850..27377252hg19UCSC Ensembl
Outerchr4:27071732..27387195hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38315464
hg19315464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014122
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156129
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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