A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5084n100



Internal ID22791171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:3876051..4182551hg38UCSC Ensembl
chr4:3877778..4184278hg19UCSC Ensembl
chr4:3847576..4235179hg18UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38306501
hg19306501
hg18387604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005566, nsv999919, nsv999754, nsv1005868, nsv1010973, nsv1013748, nsv1007135, nsv1009515, nsv1009901, nsv1004434, nsv1008883, nsv997656, nsv1007614, nsv998453, nsv1009623, nsv1002732, nsv1004915, nsv1012613, nsv1009122, nsv1007512
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)dgv5084n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss27
Observed Complex0
Frequencyn/a


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