A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156157



Internal ID22086662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:48133591..48157298hg38UCSC Ensembl
Outerchr4:48125504..48157334hg38UCSC Ensembl
Innerchr4:48135608..48159315hg19UCSC Ensembl
Outerchr4:48127521..48159351hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg3831831
hg1931831
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014249
Samples
Known GenesTEC, TXK
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156157
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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