A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014729



Internal ID22076360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:96399079..96401252hg38UCSC Ensembl
Outerchr4:96395896..96405817hg38UCSC Ensembl
Innerchr4:97320230..97322403hg19UCSC Ensembl
Outerchr4:97317047..97326968hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg389922
hg199922
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156202
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014729
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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