A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156151



Internal ID22086656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:42713580..42829171hg38UCSC Ensembl
Outerchr4:42696259..42829805hg38UCSC Ensembl
Innerchr4:42715597..42831188hg19UCSC Ensembl
Outerchr4:42698276..42831822hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38133547
hg19133547
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014243
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156151
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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