A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5821n100



Internal ID20157437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:155473737..155498618hg38UCSC Ensembl
chr5:154853297..154878178hg19UCSC Ensembl
chr5:154833490..154858371hg18UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3824882
hg1924882
hg1824882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016612, nsv1032192, nsv1020813, nsv1033493, nsv1015532, nsv1029860
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)dgv5821n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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