A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3117n100



Internal ID22789204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:19591492..19640964hg38UCSC Ensembl
chr17:19494805..19544277hg19UCSC Ensembl
chr17:19435397..19484869hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3849473
hg1949473
hg1849473
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1060185, nsv1062843, nsv1064042, nsv1056780, nsv1063104, nsv1056466, nsv1059856, nsv1055871, nsv1058837, nsv1060819, nsv1062609, nsv1061056, nsv1064221, nsv1056853, nsv1064603, nsv1061005, nsv1059269, nsv1065299, nsv1058288, nsv1061339, nsv1063775, nsv1059515, nsv1056213
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)dgv3117n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss357
Observed Complex0
Frequencyn/a


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