A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007891



Internal ID18750422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:86309448..86331371hg38UCSC Ensembl
Innerchr4:87230601..87252524hg19UCSC Ensembl
Innerchr4:87449625..87471548hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3821924
hg1921924
hg1821924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633923
Samples
Known GenesMAPK10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007891
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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