A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015660



Internal ID22077291
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:141297594..141301887hg38UCSC Ensembl
Outerchr4:141295068..141309585hg38UCSC Ensembl
Innerchr4:142218748..142223041hg19UCSC Ensembl
Outerchr4:142216222..142230739hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3814518
hg1914518
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156235
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015660
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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