A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1002648



Internal ID15949918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86056124..86058430hg38UCSC Ensembl
Innerchr4:86977277..86979583hg19UCSC Ensembl
Innerchr4:87196301..87198607hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg382307
hg192307
hg182307
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv594766
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)nssv1002648
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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