A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6803n100



Internal ID22792890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:1570505..1665298hg38UCSC Ensembl
chr8:1518671..1613464hg19UCSC Ensembl
chr8:1506078..1600871hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3894794
hg1994794
hg1894794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018421, nsv1031784, nsv1027685
Samples
Known GenesDLGAP2, LOC100507435
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6803n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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