A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3093n100



Internal ID20154709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6384798..6415931hg38UCSC Ensembl
chr17:6288118..6319251hg19UCSC Ensembl
chr17:6228842..6259975hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3831134
hg1931134
hg1831134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1063044, nsv1058878, nsv1067227
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)dgv3093n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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