A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4014714



Internal ID22076345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86054941..86065375hg38UCSC Ensembl
Outerchr4:86054070..86069538hg38UCSC Ensembl
Innerchr4:86976094..86986528hg19UCSC Ensembl
Outerchr4:86975223..86990691hg19UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3815469
hg1915469
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156194
Supporting Variants
Samples
Known GenesMAPK10
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4014714
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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