A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4017674



Internal ID22079305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:89345442..89370231hg38UCSC Ensembl
Outerchr3:89337951..89370771hg38UCSC Ensembl
Innerchr3:89394592..89419381hg19UCSC Ensembl
Outerchr3:89387101..89419921hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3832821
hg1932821
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156000
Supporting Variants
Samples
Known GenesEPHA3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4017674
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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