A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5816n100



Internal ID22791903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:145147630..145190494hg38UCSC Ensembl
chr5:144527193..144570057hg19UCSC Ensembl
chr5:144507386..144550250hg18UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3842865
hg1942865
hg1842865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030271, nsv1026188
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)dgv5816n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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