A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002646



Internal ID15949916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86056124..86058256hg38UCSC Ensembl
Innerchr4:86977277..86979409hg19UCSC Ensembl
Innerchr4:87196301..87198433hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg382133
hg192133
hg182133
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594765
Supporting Variants
Samples
Known GenesMAPK10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1002646
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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