A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv446n100



Internal ID20152062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159992675..160020138hg38UCSC Ensembl
chr1:159962465..159989928hg19UCSC Ensembl
chr1:158229089..158256552hg18UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg3827464
hg1927464
hg1827464
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000569, nsv1007787
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)dgv446n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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