A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7001n100



Internal ID22793088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:8197726..8298706hg38UCSC Ensembl
chr8:8055248..8156228hg19UCSC Ensembl
chr8:8092658..8193638hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38100981
hg19100981
hg18100981
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022805, nsv1032566, nsv1027134, nsv1021458, nsv1028595, nsv1031855
Samples
Known GenesFAM86B3P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7001n100
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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