A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156437



Internal ID22086838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:314962..351376hg38UCSC Ensembl
Outerchr6:303121..354489hg38UCSC Ensembl
Innerchr6:314962..351376hg19UCSC Ensembl
Outerchr6:303121..354489hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3851369
hg1951369
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018290
Samples
Known GenesDUSP22
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156437
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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