A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5332n100



Internal ID20156948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86044950..86062079hg38UCSC Ensembl
chr4:86966103..86983232hg19UCSC Ensembl
chr4:87185127..87202256hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3817130
hg1917130
hg1817130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1004688, nsv998531
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)dgv5332n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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