A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7069n100



Internal ID22793156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12403406..12520766hg38UCSC Ensembl
chr8:12260915..12378275hg19UCSC Ensembl
chr8:12305286..12422646hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38117361
hg19117361
hg18117361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022386, nsv1029359, nsv1022917, nsv1019864, nsv1028121, nsv1023201, nsv1031840, nsv1016046
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7069n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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