A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156115



Internal ID22086620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:10652646..10725229hg38UCSC Ensembl
Outerchr4:10651633..10726950hg38UCSC Ensembl
Innerchr4:10654270..10726853hg19UCSC Ensembl
Outerchr4:10653257..10728574hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3875318
hg1975318
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014095
Samples
Known GenesCLNK
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156115
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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