A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5646n100



Internal ID22791733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:46106721..46334765hg38UCSC Ensembl
chr5:46106823..46334867hg19UCSC Ensembl
chr5:46142580..46370624hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38228045
hg19228045
hg18228045
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019323, nsv1030599, nsv1020434
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)dgv5646n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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