A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5388n100



Internal ID22791475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:131009759..131443017hg38UCSC Ensembl
chr4:131930914..132364172hg19UCSC Ensembl
chr4:132150364..132583622hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38433259
hg19433259
hg18433259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033997, nsv1025999, nsv1028443, nsv1029281, nsv1028845, nsv1016445, nsv1019936, nsv1035008, nsv1026698, nsv1017923, nsv1020809, nsv1033631
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5388n100
Frequency
Sample Size11257
Observed Gain28
Observed Loss0
Observed Complex0
Frequencyn/a


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