A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5599n100



Internal ID22791686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20886606..21325152hg38UCSC Ensembl
chr5:20886715..21325261hg19UCSC Ensembl
chr5:20922472..21361018hg18UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38438547
hg19438547
hg18438547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018496, nsv1024176
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)dgv5599n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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