A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5569n100



Internal ID22791656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10833580..10964559hg38UCSC Ensembl
chr5:10833692..10964671hg19UCSC Ensembl
chr5:10886692..11017671hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38130980
hg19130980
hg18130980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033972, nsv1027810
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)dgv5569n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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