A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4016299



Internal ID22077930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4093314..4125604hg38UCSC Ensembl
Outerchr3:4092560..4132155hg38UCSC Ensembl
Innerchr3:4134998..4167288hg19UCSC Ensembl
Outerchr3:4134244..4173839hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3839596
hg1939596
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155948
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4016299
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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