A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5831n100



Internal ID22791918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172645828..172753954hg38UCSC Ensembl
chr5:172072831..172180957hg19UCSC Ensembl
chr5:172005436..172113562hg18UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38108127
hg19108127
hg18108127
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1027335, nsv1015884, nsv1031020, nsv1018080, nsv1016133, nsv1034109, nsv1018207, nsv1024885, nsv1020326, nsv1016535, nsv1017421
Samples
Known GenesNEURL1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5831n100
Frequency
Sample Size11257
Observed Gain13
Observed Loss0
Observed Complex0
Frequencyn/a


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