A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5436n100



Internal ID20157052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:150743286..151150724hg38UCSC Ensembl
chr4:151664438..152071876hg19UCSC Ensembl
chr4:151883888..152291326hg18UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38407439
hg19407439
hg18407439
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015387, nsv1017850, nsv1031720, nsv1018404
Samples
Known GenesLRBA, RPS3A, SH3D19, SNORD73A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5436n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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