A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5919n100



Internal ID22792006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15026899..15063559hg38UCSC Ensembl
chr6:15027130..15063790hg19UCSC Ensembl
chr6:15135109..15171769hg18UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3836661
hg1936661
hg1836661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1015671, nsv1026368
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)dgv5919n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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