A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156193



Internal ID22086698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86054941..86058791hg38UCSC Ensembl
Outerchr4:86054070..86058936hg38UCSC Ensembl
Innerchr4:86976094..86979944hg19UCSC Ensembl
Outerchr4:86975223..86980089hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg384867
hg194867
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4014712, nssv4014713
Samples
Known GenesMAPK10
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156193
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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