A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3279n100



Internal ID22789366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:71190740..71263171hg38UCSC Ensembl
chr17:69186881..69259312hg19UCSC Ensembl
chr17:66698476..66770907hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3872432
hg1972432
hg1872432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064836, nsv1066746, nsv1061994
Samples
Known GenesCASC17
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3279n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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