A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6093n100



Internal ID20157709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93743198..93875011hg38UCSC Ensembl
chr6:94452916..94584729hg19UCSC Ensembl
chr6:94509637..94641450hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38131814
hg19131814
hg18131814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019452, nsv1018160
Samples
Known GenesTSG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6093n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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