A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5826n100



Internal ID22791913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:163314374..163381222hg38UCSC Ensembl
chr5:162741380..162808228hg19UCSC Ensembl
chr5:162673958..162740806hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3866849
hg1966849
hg1866849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022560, nsv1033825, nsv1029350, nsv1026047
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)dgv5826n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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