A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5588n100



Internal ID22791675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17601432..17744476hg38UCSC Ensembl
chr5:17601541..17744585hg19UCSC Ensembl
chr5:17644644..17780317hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38143045
hg19143045
hg18135674
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034866, nsv1020396, nsv1016601, nsv1017075, nsv1033862
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)dgv5588n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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