A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014732



Internal ID22076363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:97251263..97263981hg38UCSC Ensembl
Outerchr4:97250644..97267978hg38UCSC Ensembl
Innerchr4:98172414..98185132hg19UCSC Ensembl
Outerchr4:98171795..98189129hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3817335
hg1917335
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156204
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014732
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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