A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5334n100



Internal ID20156950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86054929..86079056hg38UCSC Ensembl
chr4:86976082..87000209hg19UCSC Ensembl
chr4:87195106..87219233hg18UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg3824128
hg1924128
hg1824128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000186, nsv1006616
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)dgv5334n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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