A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4408



Internal ID15202428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:86131114..86147593hg38UCSC Ensembl
Outerchr4:87052267..87068746hg19UCSC Ensembl
Outerchr4:87271291..87287770hg18UCSC Ensembl
Outerchr4:87409446..87425925hg17UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg386096
hg196096
hg186096
hg176096
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7976
SamplesNA12156
Known GenesMAPK10
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv4408
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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