A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4015898



Internal ID22077529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:143050037..143076956hg38UCSC Ensembl
Outerchr3:143046124..143081405hg38UCSC Ensembl
Innerchr3:142768879..142795798hg19UCSC Ensembl
Outerchr3:142764966..142800247hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3835282
hg1935282
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156022
Supporting Variants
Samples
Known GenesU2SURP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4015898
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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