A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014122



Internal ID22075753
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156129
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014122
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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