A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156455



Internal ID22086856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:4670863..4679979hg38UCSC Ensembl
Outerchr6:4666879..4682784hg38UCSC Ensembl
Innerchr6:4671097..4680213hg19UCSC Ensembl
Outerchr6:4667113..4683018hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg3815906
hg1915906
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018309
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156455
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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