A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594760



Internal ID16035483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86055260..86058774hg38UCSC Ensembl
Innerchr4:86976413..86979927hg19UCSC Ensembl
Innerchr4:87195437..87198951hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg383515
hg193515
hg183515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1002637, nssv1002636, nssv1002639, nssv1002638
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594760
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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