A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156023



Internal ID22086528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:146876137..147011131hg38UCSC Ensembl
Outerchr3:146871024..147018252hg38UCSC Ensembl
Innerchr3:146593924..146728918hg19UCSC Ensembl
Outerchr3:146588811..146736039hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38147229
hg19147229
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4015899
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156023
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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