A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594774



Internal ID16035497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86056551..86058205hg38UCSC Ensembl
Innerchr4:86977704..86979358hg19UCSC Ensembl
Innerchr4:87196728..87198382hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg381655
hg191655
hg181655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9148n54
Supporting Variantsnssv1002737
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594774
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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