A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5089n100



Internal ID22791176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3912156..4173838hg38UCSC Ensembl
chr4:3913883..4175565hg19UCSC Ensembl
chr4:3964803..4226466hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38261683
hg19261683
hg18261664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001848, nsv1012159, nsv1008706, nsv1012653, nsv1004617, nsv999899
Samples
Known GenesFAM86EP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5089n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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