A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3278n100



Internal ID22789365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70439015..70639700hg38UCSC Ensembl
chr17:68435156..68635841hg19UCSC Ensembl
chr17:65946751..66147436hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg38200686
hg19200686
hg18200686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063533, nsv1063095
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)dgv3278n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer