A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3267n100



Internal ID22789354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:56078491..56096102hg38UCSC Ensembl
chr17:54155852..54173463hg19UCSC Ensembl
chr17:51510851..51528462hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3817612
hg1917612
hg1817612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1064572, nsv1061429, nsv1060006, nsv1058859, nsv1060558, nsv1067023, nsv1064933, nsv1066688, nsv1055819, nsv1056199, nsv1060945, nsv1065824, nsv1055987
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)dgv3267n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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