A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3078n100



Internal ID20154694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:842299..987971hg38UCSC Ensembl
chr17:745539..891211hg19UCSC Ensembl
chr17:692289..837961hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38145673
hg19145673
hg18145673
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058467, nsv1059428
Samples
Known GenesNXN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3078n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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