A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154726



Internal ID22085231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:219338267..219446196hg38UCSC Ensembl
Outerchr1:219334331..219450253hg38UCSC Ensembl
Innerchr1:219511609..219619538hg19UCSC Ensembl
Outerchr1:219507673..219623595hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38115923
hg19115923
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4007961
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154726
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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