A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5333n100



Internal ID20156949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86053362..86070837hg38UCSC Ensembl
chr4:86974515..86991990hg19UCSC Ensembl
chr4:87193539..87211014hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3817476
hg1917476
hg1817476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005458, nsv999551, nsv1011713
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)dgv5333n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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