A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594757



Internal ID16035480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86053909..86058099hg38UCSC Ensembl
Innerchr4:86975062..86979252hg19UCSC Ensembl
Innerchr4:87194086..87198276hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg384191
hg194191
hg184191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9146n54
Supporting Variantsnssv1002633
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594757
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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