A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7200n100



Internal ID22793287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:45935900..46151810hg38UCSC Ensembl
chr8:46847522..47063432hg19UCSC Ensembl
chr8:46966687..47182597hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg38215911
hg19215911
hg18215911
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017900, nsv1028273
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)dgv7200n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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