A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3091n100



Internal ID22789178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6203166..6235439hg38UCSC Ensembl
chr17:6106486..6138759hg19UCSC Ensembl
chr17:6047210..6079483hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3832274
hg1932274
hg1832274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1066241, nsv1059047, nsv1056520, nsv1060162, nsv1057129, nsv1058269, nsv1055835, nsv1057082, nsv1059445, nsv1057044, nsv1066483, nsv1063963, nsv1058437
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)dgv3091n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss157
Observed Complex0
Frequencyn/a


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