A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5556n100



Internal ID22791643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:5680475..5736528hg38UCSC Ensembl
chr5:5680588..5736641hg19UCSC Ensembl
chr5:5733588..5789641hg18UCSC Ensembl
Cytoband5p15.32
Allele length
AssemblyAllele length
hg3856054
hg1956054
hg1856054
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1021137, nsv1032656
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)dgv5556n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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