A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594781



Internal ID16035504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86057674..86058695hg38UCSC Ensembl
Innerchr4:86978827..86979848hg19UCSC Ensembl
Innerchr4:87197851..87198872hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg381022
hg191022
hg181022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9150n54
Supporting Variantsnssv1002751
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594781
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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