A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3094n100



Internal ID22789181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6388017..6411858hg38UCSC Ensembl
chr17:6291337..6315178hg19UCSC Ensembl
chr17:6232061..6255902hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3823842
hg1923842
hg1823842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064679, nsv1058111, nsv1062320, nsv1058449, nsv1067269, nsv1067358
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)dgv3094n100
Frequency
Sample Size11257
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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